A gene (ETM) for essential tremor maps to chromosome 2p22-p25

We report the results of linkage analysis in a large American family of Czech descent with dominantly inherited “Pure” essential tremor (ET) and genetic anticipation. Genetic loci on chromosome 2p22‐p25 establish linkage to this region with a maximum LOD score (Zmax) = 5.92 for the locus, D2S272. Ob...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Movement disorders 1997-11, Vol.12 (6), p.859-864
Hauptverfasser: Higgins, Joseph J., Pho, Lana T., Nee, Linda E.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 864
container_issue 6
container_start_page 859
container_title Movement disorders
container_volume 12
creator Higgins, Joseph J.
Pho, Lana T.
Nee, Linda E.
description We report the results of linkage analysis in a large American family of Czech descent with dominantly inherited “Pure” essential tremor (ET) and genetic anticipation. Genetic loci on chromosome 2p22‐p25 establish linkage to this region with a maximum LOD score (Zmax) = 5.92 for the locus, D2S272. Obligate recombinant events place the ETM gene in a 15‐cM candidate interval between the genetic loci D2S168 and D2S224. Repeat expansion detection analysis suggests that expanded CAG trinucleotide sequences are associated with ET. These findings will facilitate the search for an ETM gene and may further our understanding of the human motor system.
doi_str_mv 10.1002/mds.870120605
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79461448</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>79461448</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5085-934068a2edc0e678ecbeea0644a09cf0bf32a26be75274404601b403e7cf86573</originalsourceid><addsrcrecordid>eNp9kL1LxEAQxRdR9PwoLYUUIlpEZ783hYX4DacWnlgum72JRpNL3M2h_vdGLhxWVgPzfvPm8QjZpXBMAdhJPY3HRgNloECukBGVnKaGSb1KRmCMTDk1coNsxvgGQKmkap2sZzzLGOgROT1LXnCGyeHl5O4oKZqQYIw460pXJV3Aul_Uro1J1yT-NTR1E5saE9YylrZMbpO1wlURd4a5RZ6uLifnN-n44fr2_Gycegl9gowLUMYxnHpApQ36HNGBEsJB5gvIC84cUzlqybQQIBTQXABH7QujpOZb5GDh24bmY46xs3UZPVaVm2Ezj1ZnQlEhTA-mC9CHJsaAhW1DWbvwbSnY37psX5dd1tXze4PxPK9xuqSHfnp9f9Bd9K4qgpv5Mi4xBlIJTXtML7DPssLv_3_au4vHvwGGwGXs8Gt56cK7VZpraZ_vr-0zvaeTi8nYav4DSFmOeg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>79461448</pqid></control><display><type>article</type><title>A gene (ETM) for essential tremor maps to chromosome 2p22-p25</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Higgins, Joseph J. ; Pho, Lana T. ; Nee, Linda E.</creator><creatorcontrib>Higgins, Joseph J. ; Pho, Lana T. ; Nee, Linda E.</creatorcontrib><description>We report the results of linkage analysis in a large American family of Czech descent with dominantly inherited “Pure” essential tremor (ET) and genetic anticipation. Genetic loci on chromosome 2p22‐p25 establish linkage to this region with a maximum LOD score (Zmax) = 5.92 for the locus, D2S272. Obligate recombinant events place the ETM gene in a 15‐cM candidate interval between the genetic loci D2S168 and D2S224. Repeat expansion detection analysis suggests that expanded CAG trinucleotide sequences are associated with ET. These findings will facilitate the search for an ETM gene and may further our understanding of the human motor system.</description><identifier>ISSN: 0885-3185</identifier><identifier>EISSN: 1531-8257</identifier><identifier>DOI: 10.1002/mds.870120605</identifier><identifier>PMID: 9399207</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; Adult ; Aged ; Biological and medical sciences ; Child ; Chromosome Aberrations - genetics ; Chromosome Disorders ; Chromosomes, Human, Pair 2 - genetics ; Czech Republic - ethnology ; Essential tremor ; Genetic Linkage - genetics ; Haplotypes - genetics ; Human chromosome 2p ; Humans ; Linkage analysis ; Medical sciences ; Middle Aged ; Nervous system (semeiology, syndromes) ; Nervous system as a whole ; Neurology ; Pedigree ; Phenotype ; Severity of Illness Index ; Tremor - diagnosis ; Tremor - genetics ; Trinucleotide Repeats - genetics ; United States ; X Chromosome</subject><ispartof>Movement disorders, 1997-11, Vol.12 (6), p.859-864</ispartof><rights>Copyright © 1997 Movement Disorder Society</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5085-934068a2edc0e678ecbeea0644a09cf0bf32a26be75274404601b403e7cf86573</citedby><cites>FETCH-LOGICAL-c5085-934068a2edc0e678ecbeea0644a09cf0bf32a26be75274404601b403e7cf86573</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmds.870120605$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmds.870120605$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2056471$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9399207$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Higgins, Joseph J.</creatorcontrib><creatorcontrib>Pho, Lana T.</creatorcontrib><creatorcontrib>Nee, Linda E.</creatorcontrib><title>A gene (ETM) for essential tremor maps to chromosome 2p22-p25</title><title>Movement disorders</title><addtitle>Mov. Disord</addtitle><description>We report the results of linkage analysis in a large American family of Czech descent with dominantly inherited “Pure” essential tremor (ET) and genetic anticipation. Genetic loci on chromosome 2p22‐p25 establish linkage to this region with a maximum LOD score (Zmax) = 5.92 for the locus, D2S272. Obligate recombinant events place the ETM gene in a 15‐cM candidate interval between the genetic loci D2S168 and D2S224. Repeat expansion detection analysis suggests that expanded CAG trinucleotide sequences are associated with ET. These findings will facilitate the search for an ETM gene and may further our understanding of the human motor system.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Chromosome Aberrations - genetics</subject><subject>Chromosome Disorders</subject><subject>Chromosomes, Human, Pair 2 - genetics</subject><subject>Czech Republic - ethnology</subject><subject>Essential tremor</subject><subject>Genetic Linkage - genetics</subject><subject>Haplotypes - genetics</subject><subject>Human chromosome 2p</subject><subject>Humans</subject><subject>Linkage analysis</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Nervous system as a whole</subject><subject>Neurology</subject><subject>Pedigree</subject><subject>Phenotype</subject><subject>Severity of Illness Index</subject><subject>Tremor - diagnosis</subject><subject>Tremor - genetics</subject><subject>Trinucleotide Repeats - genetics</subject><subject>United States</subject><subject>X Chromosome</subject><issn>0885-3185</issn><issn>1531-8257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kL1LxEAQxRdR9PwoLYUUIlpEZ783hYX4DacWnlgum72JRpNL3M2h_vdGLhxWVgPzfvPm8QjZpXBMAdhJPY3HRgNloECukBGVnKaGSb1KRmCMTDk1coNsxvgGQKmkap2sZzzLGOgROT1LXnCGyeHl5O4oKZqQYIw460pXJV3Aul_Uro1J1yT-NTR1E5saE9YylrZMbpO1wlURd4a5RZ6uLifnN-n44fr2_Gycegl9gowLUMYxnHpApQ36HNGBEsJB5gvIC84cUzlqybQQIBTQXABH7QujpOZb5GDh24bmY46xs3UZPVaVm2Ezj1ZnQlEhTA-mC9CHJsaAhW1DWbvwbSnY37psX5dd1tXze4PxPK9xuqSHfnp9f9Bd9K4qgpv5Mi4xBlIJTXtML7DPssLv_3_au4vHvwGGwGXs8Gt56cK7VZpraZ_vr-0zvaeTi8nYav4DSFmOeg</recordid><startdate>199711</startdate><enddate>199711</enddate><creator>Higgins, Joseph J.</creator><creator>Pho, Lana T.</creator><creator>Nee, Linda E.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><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>7X8</scope><scope>8BM</scope></search><sort><creationdate>199711</creationdate><title>A gene (ETM) for essential tremor maps to chromosome 2p22-p25</title><author>Higgins, Joseph J. ; Pho, Lana T. ; Nee, Linda E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5085-934068a2edc0e678ecbeea0644a09cf0bf32a26be75274404601b403e7cf86573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Chromosome Aberrations - genetics</topic><topic>Chromosome Disorders</topic><topic>Chromosomes, Human, Pair 2 - genetics</topic><topic>Czech Republic - ethnology</topic><topic>Essential tremor</topic><topic>Genetic Linkage - genetics</topic><topic>Haplotypes - genetics</topic><topic>Human chromosome 2p</topic><topic>Humans</topic><topic>Linkage analysis</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Nervous system as a whole</topic><topic>Neurology</topic><topic>Pedigree</topic><topic>Phenotype</topic><topic>Severity of Illness Index</topic><topic>Tremor - diagnosis</topic><topic>Tremor - genetics</topic><topic>Trinucleotide Repeats - genetics</topic><topic>United States</topic><topic>X Chromosome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Higgins, Joseph J.</creatorcontrib><creatorcontrib>Pho, Lana T.</creatorcontrib><creatorcontrib>Nee, Linda E.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>ComDisDome</collection><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Higgins, Joseph J.</au><au>Pho, Lana T.</au><au>Nee, Linda E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A gene (ETM) for essential tremor maps to chromosome 2p22-p25</atitle><jtitle>Movement disorders</jtitle><addtitle>Mov. Disord</addtitle><date>1997-11</date><risdate>1997</risdate><volume>12</volume><issue>6</issue><spage>859</spage><epage>864</epage><pages>859-864</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>We report the results of linkage analysis in a large American family of Czech descent with dominantly inherited “Pure” essential tremor (ET) and genetic anticipation. Genetic loci on chromosome 2p22‐p25 establish linkage to this region with a maximum LOD score (Zmax) = 5.92 for the locus, D2S272. Obligate recombinant events place the ETM gene in a 15‐cM candidate interval between the genetic loci D2S168 and D2S224. Repeat expansion detection analysis suggests that expanded CAG trinucleotide sequences are associated with ET. These findings will facilitate the search for an ETM gene and may further our understanding of the human motor system.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>9399207</pmid><doi>10.1002/mds.870120605</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0885-3185
ispartof Movement disorders, 1997-11, Vol.12 (6), p.859-864
issn 0885-3185
1531-8257
language eng
recordid cdi_proquest_miscellaneous_79461448
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adolescent
Adult
Aged
Biological and medical sciences
Child
Chromosome Aberrations - genetics
Chromosome Disorders
Chromosomes, Human, Pair 2 - genetics
Czech Republic - ethnology
Essential tremor
Genetic Linkage - genetics
Haplotypes - genetics
Human chromosome 2p
Humans
Linkage analysis
Medical sciences
Middle Aged
Nervous system (semeiology, syndromes)
Nervous system as a whole
Neurology
Pedigree
Phenotype
Severity of Illness Index
Tremor - diagnosis
Tremor - genetics
Trinucleotide Repeats - genetics
United States
X Chromosome
title A gene (ETM) for essential tremor maps to chromosome 2p22-p25
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T12%3A53%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20gene%20(ETM)%20for%20essential%20tremor%20maps%20to%20chromosome%202p22-p25&rft.jtitle=Movement%20disorders&rft.au=Higgins,%20Joseph%20J.&rft.date=1997-11&rft.volume=12&rft.issue=6&rft.spage=859&rft.epage=864&rft.pages=859-864&rft.issn=0885-3185&rft.eissn=1531-8257&rft_id=info:doi/10.1002/mds.870120605&rft_dat=%3Cproquest_cross%3E79461448%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=79461448&rft_id=info:pmid/9399207&rfr_iscdi=true