Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis
Gespeichert in:
| Veröffentlicht in: | Nature genetics 2010-06, Vol.42 (6), p.469-470 |
|---|---|
| Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 470 |
|---|---|
| container_issue | 6 |
| container_start_page | 469 |
| container_title | Nature genetics |
| container_volume | 42 |
| creator | Booth, David R Heard, Robert N Stewart, Graeme J Cox, Mathew Scott, Rodney J Lechner-Scott, Jeannette Goris, An Dobosi, Rita Dubois, Bénédicte Saarela, Janna Leppä, Virpi Peltonen, Leena Pirttila, Tuula Cournu-Rebeix, Isabelle Fontaine, Bertrand Bergamaschi, Laura D'Alfonso, Sandra Leone, Maurizio Lorentzen, Aslaug R Harbo, Hanne F Celius, Elisabeth G Spurkland, Anne Link, Jenny Kockum, Ingrid Olsson, Tomas Hillert, Jan Ban, Maria Baker, Amie Kemppinen, Anu Sawcer, Stephen Compston, Alastair Robertson, Neil P De Jager, Philip L Hafler, David A Barcellos, Lisa F Ivinson, Adrian J McCauley, Jacob L Pericak-Vance, Margaret A Oksenberg, Jorge R Hauser, Stephen L Sexton, David Haines, Jonathan |
| description | |
| doi_str_mv | 10.1038/ng0610-469 |
| format | Article |
| fullrecord | <record><control><sourceid>gale_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_swepub_ki_se_551083</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A227945834</galeid><sourcerecordid>A227945834</sourcerecordid><originalsourceid>FETCH-LOGICAL-c586t-1d485f29678b2f5a02addaf9e0733ccb6a5e29bef9e19cee66a453def2e5bb793</originalsourceid><addsrcrecordid>eNqNkk1v1DAQhiMEoqVw4QcgSxwQoBTbsfNxQSorCitWqsTXBYHlOOPUbWIvttPCv8erLBWRekA-ePTOM-9h5s2yxwQfE1zUr2yPS4JzVjZ3skPCWZmTitR3U530nOGiPMgehHCBMWEM1_ezA4o5pqxmh9mPjVSXyGkUpu3W-Yi080iG4JSR0TiLWojXABbFc0Af1qfkDfKBYNbQpqLfVt_RlfRG2oik7dA4DdFsB0BBDeBdMOFhdk_LIcCj_X-UfTl9-3n1Pt-cvVuvTja54nUZc9KxmmvalFXdUs0lprLrpG4AV0WhVFtKDrRpISmkUQBlKRkvOtAUeNtWTXGU5bNvuIbt1IqtN6P0v4WTRuyly1SB4Jzgukj865lPnRE6BTZ6OSzGlh1rzkXvrkRBcFNXO4NnewPvfk4QohhNUDAM0oKbgqhYSQtWVSSRT2eylwMIY7VLhmpHixNKq4bxumCJOr6FSq-D0ShnQZukLwaeLwYSE-FX7OUUglh_-vj_7NnXJftiZlU6YPCgb5ZCsNjFTcxxEyluCX7y7xpv0L_5SsDL_V1Sy_bgxYWbvE1RuM3uD3q43F4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>746234771</pqid></control><display><type>article</type><title>Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis</title><source>MEDLINE</source><source>SpringerLink Journals</source><source>Nature Journals Online</source><source>SWEPUB Freely available online</source><creator>Booth, David R ; Heard, Robert N ; Stewart, Graeme J ; Cox, Mathew ; Scott, Rodney J ; Lechner-Scott, Jeannette ; Goris, An ; Dobosi, Rita ; Dubois, Bénédicte ; Saarela, Janna ; Leppä, Virpi ; Peltonen, Leena ; Pirttila, Tuula ; Cournu-Rebeix, Isabelle ; Fontaine, Bertrand ; Bergamaschi, Laura ; D'Alfonso, Sandra ; Leone, Maurizio ; Lorentzen, Aslaug R ; Harbo, Hanne F ; Celius, Elisabeth G ; Spurkland, Anne ; Link, Jenny ; Kockum, Ingrid ; Olsson, Tomas ; Hillert, Jan ; Ban, Maria ; Baker, Amie ; Kemppinen, Anu ; Sawcer, Stephen ; Compston, Alastair ; Robertson, Neil P ; De Jager, Philip L ; Hafler, David A ; Barcellos, Lisa F ; Ivinson, Adrian J ; McCauley, Jacob L ; Pericak-Vance, Margaret A ; Oksenberg, Jorge R ; Hauser, Stephen L ; Sexton, David ; Haines, Jonathan</creator><creatorcontrib>Booth, David R ; Heard, Robert N ; Stewart, Graeme J ; Cox, Mathew ; Scott, Rodney J ; Lechner-Scott, Jeannette ; Goris, An ; Dobosi, Rita ; Dubois, Bénédicte ; Saarela, Janna ; Leppä, Virpi ; Peltonen, Leena ; Pirttila, Tuula ; Cournu-Rebeix, Isabelle ; Fontaine, Bertrand ; Bergamaschi, Laura ; D'Alfonso, Sandra ; Leone, Maurizio ; Lorentzen, Aslaug R ; Harbo, Hanne F ; Celius, Elisabeth G ; Spurkland, Anne ; Link, Jenny ; Kockum, Ingrid ; Olsson, Tomas ; Hillert, Jan ; Ban, Maria ; Baker, Amie ; Kemppinen, Anu ; Sawcer, Stephen ; Compston, Alastair ; Robertson, Neil P ; De Jager, Philip L ; Hafler, David A ; Barcellos, Lisa F ; Ivinson, Adrian J ; McCauley, Jacob L ; Pericak-Vance, Margaret A ; Oksenberg, Jorge R ; Hauser, Stephen L ; Sexton, David ; Haines, Jonathan ; International Multiple Sclerosis Genetics Consortium (IMSGC)</creatorcontrib><identifier>ISSN: 1061-4036</identifier><identifier>EISSN: 1546-1718</identifier><identifier>DOI: 10.1038/ng0610-469</identifier><identifier>PMID: 20502484</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>631/208/457/649 ; 692/699/375/1666 ; Agriculture ; Animal Genetics and Genomics ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; correspondence ; Diagnosis ; Disease susceptibility ; Gene Function ; Genetic aspects ; Genetic Predisposition to Disease ; Genetic Variation ; Human Genetics ; Humans ; Kinesins - genetics ; Multiple sclerosis ; Multiple Sclerosis - genetics ; Risk factors ; Single nucleotide polymorphisms</subject><ispartof>Nature genetics, 2010-06, Vol.42 (6), p.469-470</ispartof><rights>Springer Nature America, Inc. 2010</rights><rights>COPYRIGHT 2010 Nature Publishing Group</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c586t-1d485f29678b2f5a02addaf9e0733ccb6a5e29bef9e19cee66a453def2e5bb793</citedby><cites>FETCH-LOGICAL-c586t-1d485f29678b2f5a02addaf9e0733ccb6a5e29bef9e19cee66a453def2e5bb793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/ng0610-469$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/ng0610-469$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,550,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20502484$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:120512849$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Booth, David R</creatorcontrib><creatorcontrib>Heard, Robert N</creatorcontrib><creatorcontrib>Stewart, Graeme J</creatorcontrib><creatorcontrib>Cox, Mathew</creatorcontrib><creatorcontrib>Scott, Rodney J</creatorcontrib><creatorcontrib>Lechner-Scott, Jeannette</creatorcontrib><creatorcontrib>Goris, An</creatorcontrib><creatorcontrib>Dobosi, Rita</creatorcontrib><creatorcontrib>Dubois, Bénédicte</creatorcontrib><creatorcontrib>Saarela, Janna</creatorcontrib><creatorcontrib>Leppä, Virpi</creatorcontrib><creatorcontrib>Peltonen, Leena</creatorcontrib><creatorcontrib>Pirttila, Tuula</creatorcontrib><creatorcontrib>Cournu-Rebeix, Isabelle</creatorcontrib><creatorcontrib>Fontaine, Bertrand</creatorcontrib><creatorcontrib>Bergamaschi, Laura</creatorcontrib><creatorcontrib>D'Alfonso, Sandra</creatorcontrib><creatorcontrib>Leone, Maurizio</creatorcontrib><creatorcontrib>Lorentzen, Aslaug R</creatorcontrib><creatorcontrib>Harbo, Hanne F</creatorcontrib><creatorcontrib>Celius, Elisabeth G</creatorcontrib><creatorcontrib>Spurkland, Anne</creatorcontrib><creatorcontrib>Link, Jenny</creatorcontrib><creatorcontrib>Kockum, Ingrid</creatorcontrib><creatorcontrib>Olsson, Tomas</creatorcontrib><creatorcontrib>Hillert, Jan</creatorcontrib><creatorcontrib>Ban, Maria</creatorcontrib><creatorcontrib>Baker, Amie</creatorcontrib><creatorcontrib>Kemppinen, Anu</creatorcontrib><creatorcontrib>Sawcer, Stephen</creatorcontrib><creatorcontrib>Compston, Alastair</creatorcontrib><creatorcontrib>Robertson, Neil P</creatorcontrib><creatorcontrib>De Jager, Philip L</creatorcontrib><creatorcontrib>Hafler, David A</creatorcontrib><creatorcontrib>Barcellos, Lisa F</creatorcontrib><creatorcontrib>Ivinson, Adrian J</creatorcontrib><creatorcontrib>McCauley, Jacob L</creatorcontrib><creatorcontrib>Pericak-Vance, Margaret A</creatorcontrib><creatorcontrib>Oksenberg, Jorge R</creatorcontrib><creatorcontrib>Hauser, Stephen L</creatorcontrib><creatorcontrib>Sexton, David</creatorcontrib><creatorcontrib>Haines, Jonathan</creatorcontrib><creatorcontrib>International Multiple Sclerosis Genetics Consortium (IMSGC)</creatorcontrib><title>Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis</title><title>Nature genetics</title><addtitle>Nat Genet</addtitle><addtitle>Nat Genet</addtitle><subject>631/208/457/649</subject><subject>692/699/375/1666</subject><subject>Agriculture</subject><subject>Animal Genetics and Genomics</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>correspondence</subject><subject>Diagnosis</subject><subject>Disease susceptibility</subject><subject>Gene Function</subject><subject>Genetic aspects</subject><subject>Genetic Predisposition to Disease</subject><subject>Genetic Variation</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Kinesins - genetics</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - genetics</subject><subject>Risk factors</subject><subject>Single nucleotide polymorphisms</subject><issn>1061-4036</issn><issn>1546-1718</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNqNkk1v1DAQhiMEoqVw4QcgSxwQoBTbsfNxQSorCitWqsTXBYHlOOPUbWIvttPCv8erLBWRekA-ePTOM-9h5s2yxwQfE1zUr2yPS4JzVjZ3skPCWZmTitR3U530nOGiPMgehHCBMWEM1_ezA4o5pqxmh9mPjVSXyGkUpu3W-Yi080iG4JSR0TiLWojXABbFc0Af1qfkDfKBYNbQpqLfVt_RlfRG2oik7dA4DdFsB0BBDeBdMOFhdk_LIcCj_X-UfTl9-3n1Pt-cvVuvTja54nUZc9KxmmvalFXdUs0lprLrpG4AV0WhVFtKDrRpISmkUQBlKRkvOtAUeNtWTXGU5bNvuIbt1IqtN6P0v4WTRuyly1SB4Jzgukj865lPnRE6BTZ6OSzGlh1rzkXvrkRBcFNXO4NnewPvfk4QohhNUDAM0oKbgqhYSQtWVSSRT2eylwMIY7VLhmpHixNKq4bxumCJOr6FSq-D0ShnQZukLwaeLwYSE-FX7OUUglh_-vj_7NnXJftiZlU6YPCgb5ZCsNjFTcxxEyluCX7y7xpv0L_5SsDL_V1Sy_bgxYWbvE1RuM3uD3q43F4</recordid><startdate>20100601</startdate><enddate>20100601</enddate><creator>Booth, David R</creator><creator>Heard, Robert N</creator><creator>Stewart, Graeme J</creator><creator>Cox, Mathew</creator><creator>Scott, Rodney J</creator><creator>Lechner-Scott, Jeannette</creator><creator>Goris, An</creator><creator>Dobosi, Rita</creator><creator>Dubois, Bénédicte</creator><creator>Saarela, Janna</creator><creator>Leppä, Virpi</creator><creator>Peltonen, Leena</creator><creator>Pirttila, Tuula</creator><creator>Cournu-Rebeix, Isabelle</creator><creator>Fontaine, Bertrand</creator><creator>Bergamaschi, Laura</creator><creator>D'Alfonso, Sandra</creator><creator>Leone, Maurizio</creator><creator>Lorentzen, Aslaug R</creator><creator>Harbo, Hanne F</creator><creator>Celius, Elisabeth G</creator><creator>Spurkland, Anne</creator><creator>Link, Jenny</creator><creator>Kockum, Ingrid</creator><creator>Olsson, Tomas</creator><creator>Hillert, Jan</creator><creator>Ban, Maria</creator><creator>Baker, Amie</creator><creator>Kemppinen, Anu</creator><creator>Sawcer, Stephen</creator><creator>Compston, Alastair</creator><creator>Robertson, Neil P</creator><creator>De Jager, Philip L</creator><creator>Hafler, David A</creator><creator>Barcellos, Lisa F</creator><creator>Ivinson, Adrian J</creator><creator>McCauley, Jacob L</creator><creator>Pericak-Vance, Margaret A</creator><creator>Oksenberg, Jorge R</creator><creator>Hauser, Stephen L</creator><creator>Sexton, David</creator><creator>Haines, Jonathan</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope></search><sort><creationdate>20100601</creationdate><title>Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis</title><author>Booth, David R ; Heard, Robert N ; Stewart, Graeme J ; Cox, Mathew ; Scott, Rodney J ; Lechner-Scott, Jeannette ; Goris, An ; Dobosi, Rita ; Dubois, Bénédicte ; Saarela, Janna ; Leppä, Virpi ; Peltonen, Leena ; Pirttila, Tuula ; Cournu-Rebeix, Isabelle ; Fontaine, Bertrand ; Bergamaschi, Laura ; D'Alfonso, Sandra ; Leone, Maurizio ; Lorentzen, Aslaug R ; Harbo, Hanne F ; Celius, Elisabeth G ; Spurkland, Anne ; Link, Jenny ; Kockum, Ingrid ; Olsson, Tomas ; Hillert, Jan ; Ban, Maria ; Baker, Amie ; Kemppinen, Anu ; Sawcer, Stephen ; Compston, Alastair ; Robertson, Neil P ; De Jager, Philip L ; Hafler, David A ; Barcellos, Lisa F ; Ivinson, Adrian J ; McCauley, Jacob L ; Pericak-Vance, Margaret A ; Oksenberg, Jorge R ; Hauser, Stephen L ; Sexton, David ; Haines, Jonathan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c586t-1d485f29678b2f5a02addaf9e0733ccb6a5e29bef9e19cee66a453def2e5bb793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>631/208/457/649</topic><topic>692/699/375/1666</topic><topic>Agriculture</topic><topic>Animal Genetics and Genomics</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>correspondence</topic><topic>Diagnosis</topic><topic>Disease susceptibility</topic><topic>Gene Function</topic><topic>Genetic aspects</topic><topic>Genetic Predisposition to Disease</topic><topic>Genetic Variation</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Kinesins - genetics</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - genetics</topic><topic>Risk factors</topic><topic>Single nucleotide polymorphisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Booth, David R</creatorcontrib><creatorcontrib>Heard, Robert N</creatorcontrib><creatorcontrib>Stewart, Graeme J</creatorcontrib><creatorcontrib>Cox, Mathew</creatorcontrib><creatorcontrib>Scott, Rodney J</creatorcontrib><creatorcontrib>Lechner-Scott, Jeannette</creatorcontrib><creatorcontrib>Goris, An</creatorcontrib><creatorcontrib>Dobosi, Rita</creatorcontrib><creatorcontrib>Dubois, Bénédicte</creatorcontrib><creatorcontrib>Saarela, Janna</creatorcontrib><creatorcontrib>Leppä, Virpi</creatorcontrib><creatorcontrib>Peltonen, Leena</creatorcontrib><creatorcontrib>Pirttila, Tuula</creatorcontrib><creatorcontrib>Cournu-Rebeix, Isabelle</creatorcontrib><creatorcontrib>Fontaine, Bertrand</creatorcontrib><creatorcontrib>Bergamaschi, Laura</creatorcontrib><creatorcontrib>D'Alfonso, Sandra</creatorcontrib><creatorcontrib>Leone, Maurizio</creatorcontrib><creatorcontrib>Lorentzen, Aslaug R</creatorcontrib><creatorcontrib>Harbo, Hanne F</creatorcontrib><creatorcontrib>Celius, Elisabeth G</creatorcontrib><creatorcontrib>Spurkland, Anne</creatorcontrib><creatorcontrib>Link, Jenny</creatorcontrib><creatorcontrib>Kockum, Ingrid</creatorcontrib><creatorcontrib>Olsson, Tomas</creatorcontrib><creatorcontrib>Hillert, Jan</creatorcontrib><creatorcontrib>Ban, Maria</creatorcontrib><creatorcontrib>Baker, Amie</creatorcontrib><creatorcontrib>Kemppinen, Anu</creatorcontrib><creatorcontrib>Sawcer, Stephen</creatorcontrib><creatorcontrib>Compston, Alastair</creatorcontrib><creatorcontrib>Robertson, Neil P</creatorcontrib><creatorcontrib>De Jager, Philip L</creatorcontrib><creatorcontrib>Hafler, David A</creatorcontrib><creatorcontrib>Barcellos, Lisa F</creatorcontrib><creatorcontrib>Ivinson, Adrian J</creatorcontrib><creatorcontrib>McCauley, Jacob L</creatorcontrib><creatorcontrib>Pericak-Vance, Margaret A</creatorcontrib><creatorcontrib>Oksenberg, Jorge R</creatorcontrib><creatorcontrib>Hauser, Stephen L</creatorcontrib><creatorcontrib>Sexton, David</creatorcontrib><creatorcontrib>Haines, Jonathan</creatorcontrib><creatorcontrib>International Multiple Sclerosis Genetics Consortium (IMSGC)</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>Nature genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Booth, David R</au><au>Heard, Robert N</au><au>Stewart, Graeme J</au><au>Cox, Mathew</au><au>Scott, Rodney J</au><au>Lechner-Scott, Jeannette</au><au>Goris, An</au><au>Dobosi, Rita</au><au>Dubois, Bénédicte</au><au>Saarela, Janna</au><au>Leppä, Virpi</au><au>Peltonen, Leena</au><au>Pirttila, Tuula</au><au>Cournu-Rebeix, Isabelle</au><au>Fontaine, Bertrand</au><au>Bergamaschi, Laura</au><au>D'Alfonso, Sandra</au><au>Leone, Maurizio</au><au>Lorentzen, Aslaug R</au><au>Harbo, Hanne F</au><au>Celius, Elisabeth G</au><au>Spurkland, Anne</au><au>Link, Jenny</au><au>Kockum, Ingrid</au><au>Olsson, Tomas</au><au>Hillert, Jan</au><au>Ban, Maria</au><au>Baker, Amie</au><au>Kemppinen, Anu</au><au>Sawcer, Stephen</au><au>Compston, Alastair</au><au>Robertson, Neil P</au><au>De Jager, Philip L</au><au>Hafler, David A</au><au>Barcellos, Lisa F</au><au>Ivinson, Adrian J</au><au>McCauley, Jacob L</au><au>Pericak-Vance, Margaret A</au><au>Oksenberg, Jorge R</au><au>Hauser, Stephen L</au><au>Sexton, David</au><au>Haines, Jonathan</au><aucorp>International Multiple Sclerosis Genetics Consortium (IMSGC)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis</atitle><jtitle>Nature genetics</jtitle><stitle>Nat Genet</stitle><addtitle>Nat Genet</addtitle><date>2010-06-01</date><risdate>2010</risdate><volume>42</volume><issue>6</issue><spage>469</spage><epage>470</epage><pages>469-470</pages><issn>1061-4036</issn><eissn>1546-1718</eissn><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>20502484</pmid><doi>10.1038/ng0610-469</doi><tpages>2</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1061-4036 |
| ispartof | Nature genetics, 2010-06, Vol.42 (6), p.469-470 |
| issn | 1061-4036 1546-1718 |
| language | eng |
| recordid | cdi_swepub_primary_oai_swepub_ki_se_551083 |
| source | MEDLINE; SpringerLink Journals; Nature Journals Online; SWEPUB Freely available online |
| subjects | 631/208/457/649 692/699/375/1666 Agriculture Animal Genetics and Genomics Biomedical and Life Sciences Biomedicine Cancer Research correspondence Diagnosis Disease susceptibility Gene Function Genetic aspects Genetic Predisposition to Disease Genetic Variation Human Genetics Humans Kinesins - genetics Multiple sclerosis Multiple Sclerosis - genetics Risk factors Single nucleotide polymorphisms |
| title | Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T07%3A12%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Lack%20of%20support%20for%20association%20between%20the%20KIF1B%20rs10492972%5BC%5D%20variant%20and%20multiple%20sclerosis&rft.jtitle=Nature%20genetics&rft.au=Booth,%20David%20R&rft.aucorp=International%20Multiple%20Sclerosis%20Genetics%20Consortium%20(IMSGC)&rft.date=2010-06-01&rft.volume=42&rft.issue=6&rft.spage=469&rft.epage=470&rft.pages=469-470&rft.issn=1061-4036&rft.eissn=1546-1718&rft_id=info:doi/10.1038/ng0610-469&rft_dat=%3Cgale_swepu%3EA227945834%3C/gale_swepu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=746234771&rft_id=info:pmid/20502484&rft_galeid=A227945834&rfr_iscdi=true |