No Association Between the Putative Functional ZDHHC8 Single Nucleotide Polymorphism rs175174 and Schizophrenia in Large European Samples
It has been recently reported that a functional variant in the ZDHHC8 gene encoding a putative palmitoyltransferase directly confers susceptibility to schizophrenia in females ( Mukai et al 2004). We investigated the putative risk allele (rs175174) in four schizophrenia association samples including...
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creator | Glaser, Beate Schumacher, Johannes Williams, Hywel J. Jamra, Rami Abou Ianakiev, Nikolai Milev, Radoi Ohlraun, Stephanie Schulze, Thomas G. Czerski, Piotr M. Hauser, Joanna Jönsson, Erick G. Sedvall, Göran C. Klopp, Norman Illig, Thomas Becker, Tim Propping, Peter Williams, Nigel M. Cichon, Sven Kirov, George Rietschel, Marcella Murphy, Kieran C. O’Donovan, Michael C. Nöthen, Markus M. Owen, Michael J. |
description | It has been recently reported that a functional variant in the ZDHHC8 gene encoding a putative palmitoyltransferase directly confers susceptibility to schizophrenia in females (
Mukai et al 2004).
We investigated the putative risk allele (rs175174) in four schizophrenia association samples including a Bulgarian proband and parent sample (474 trios) and three case-control panels of European origin (1028 patients/1253 control subjects) in an attempt to replicate these findings.
Our results do not support the hypothesis that genetic variation at rs175174 is associated with increased risk for schizophrenia nor do they suggest the presence of gender-specific differences.
Our data suggest that the reported genetic association by
Mukai et al either represents type I error resulting from sampling variance or that rs175174 is in linkage disequilibrium (LD) with the functional variant for schizophrenia and different LD patterns obscure the detection of association. |
doi_str_mv | 10.1016/j.biopsych.2005.03.017 |
format | Article |
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Mukai et al 2004).
We investigated the putative risk allele (rs175174) in four schizophrenia association samples including a Bulgarian proband and parent sample (474 trios) and three case-control panels of European origin (1028 patients/1253 control subjects) in an attempt to replicate these findings.
Our results do not support the hypothesis that genetic variation at rs175174 is associated with increased risk for schizophrenia nor do they suggest the presence of gender-specific differences.
Our data suggest that the reported genetic association by
Mukai et al either represents type I error resulting from sampling variance or that rs175174 is in linkage disequilibrium (LD) with the functional variant for schizophrenia and different LD patterns obscure the detection of association.</description><identifier>ISSN: 0006-3223</identifier><identifier>EISSN: 1873-2402</identifier><identifier>DOI: 10.1016/j.biopsych.2005.03.017</identifier><identifier>PMID: 15992527</identifier><identifier>CODEN: BIPCBF</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Acyltransferases - genetics ; Adult and adolescent clinical studies ; Alleles ; Association ; Biological and medical sciences ; Bulgaria - ethnology ; Child ; chromosome 22q11 ; Chromosomes, Human, Pair 22 ; disequilibrium ; Female ; Genetic Predisposition to Disease - genetics ; Genetic Variation ; Humans ; linkage ; Linkage Disequilibrium ; Male ; Medical sciences ; Medicin och hälsovetenskap ; Membrane Proteins - genetics ; Polymorphism, Single Nucleotide - genetics ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychoses ; Reverse Transcriptase Polymerase Chain Reaction ; Risk Factors ; Schizophrenia ; Schizophrenia - enzymology ; Schizophrenia - genetics ; Sex Factors ; VCFS ; Whites - genetics ; ZDHHC8 ; Zinc Fingers - genetics</subject><ispartof>Biological psychiatry (1969), 2005-07, Vol.58 (1), p.78-80</ispartof><rights>2005 Society of Biological Psychiatry</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-8a966f0efc9815a827fe59403f62ad3172126fb3b46e9719fca46531d09ab37b3</citedby><cites>FETCH-LOGICAL-c511t-8a966f0efc9815a827fe59403f62ad3172126fb3b46e9719fca46531d09ab37b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.biopsych.2005.03.017$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16972470$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15992527$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:1942751$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Glaser, Beate</creatorcontrib><creatorcontrib>Schumacher, Johannes</creatorcontrib><creatorcontrib>Williams, Hywel J.</creatorcontrib><creatorcontrib>Jamra, Rami Abou</creatorcontrib><creatorcontrib>Ianakiev, Nikolai</creatorcontrib><creatorcontrib>Milev, Radoi</creatorcontrib><creatorcontrib>Ohlraun, Stephanie</creatorcontrib><creatorcontrib>Schulze, Thomas G.</creatorcontrib><creatorcontrib>Czerski, Piotr M.</creatorcontrib><creatorcontrib>Hauser, Joanna</creatorcontrib><creatorcontrib>Jönsson, Erick G.</creatorcontrib><creatorcontrib>Sedvall, Göran C.</creatorcontrib><creatorcontrib>Klopp, Norman</creatorcontrib><creatorcontrib>Illig, Thomas</creatorcontrib><creatorcontrib>Becker, Tim</creatorcontrib><creatorcontrib>Propping, Peter</creatorcontrib><creatorcontrib>Williams, Nigel M.</creatorcontrib><creatorcontrib>Cichon, Sven</creatorcontrib><creatorcontrib>Kirov, George</creatorcontrib><creatorcontrib>Rietschel, Marcella</creatorcontrib><creatorcontrib>Murphy, Kieran C.</creatorcontrib><creatorcontrib>O’Donovan, Michael C.</creatorcontrib><creatorcontrib>Nöthen, Markus M.</creatorcontrib><creatorcontrib>Owen, Michael J.</creatorcontrib><title>No Association Between the Putative Functional ZDHHC8 Single Nucleotide Polymorphism rs175174 and Schizophrenia in Large European Samples</title><title>Biological psychiatry (1969)</title><addtitle>Biol Psychiatry</addtitle><description>It has been recently reported that a functional variant in the ZDHHC8 gene encoding a putative palmitoyltransferase directly confers susceptibility to schizophrenia in females (
Mukai et al 2004).
We investigated the putative risk allele (rs175174) in four schizophrenia association samples including a Bulgarian proband and parent sample (474 trios) and three case-control panels of European origin (1028 patients/1253 control subjects) in an attempt to replicate these findings.
Our results do not support the hypothesis that genetic variation at rs175174 is associated with increased risk for schizophrenia nor do they suggest the presence of gender-specific differences.
Our data suggest that the reported genetic association by
Mukai et al either represents type I error resulting from sampling variance or that rs175174 is in linkage disequilibrium (LD) with the functional variant for schizophrenia and different LD patterns obscure the detection of association.</description><subject>Acyltransferases - genetics</subject><subject>Adult and adolescent clinical studies</subject><subject>Alleles</subject><subject>Association</subject><subject>Biological and medical sciences</subject><subject>Bulgaria - ethnology</subject><subject>Child</subject><subject>chromosome 22q11</subject><subject>Chromosomes, Human, Pair 22</subject><subject>disequilibrium</subject><subject>Female</subject><subject>Genetic Predisposition to Disease - genetics</subject><subject>Genetic Variation</subject><subject>Humans</subject><subject>linkage</subject><subject>Linkage Disequilibrium</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicin och hälsovetenskap</subject><subject>Membrane Proteins - genetics</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychoses</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Risk Factors</subject><subject>Schizophrenia</subject><subject>Schizophrenia - enzymology</subject><subject>Schizophrenia - genetics</subject><subject>Sex Factors</subject><subject>VCFS</subject><subject>Whites - genetics</subject><subject>ZDHHC8</subject><subject>Zinc Fingers - genetics</subject><issn>0006-3223</issn><issn>1873-2402</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v0zAYhyMEYmXwFSZf4JbiP4kd3xhlW5GqgVS4cLEc583qktjBTjaVb7Bvjat29IQ42X79PH5t_7LsguA5wYS_385r64e4M5s5xbicYzbHRDzLZqQSLKcFps-zGcaY54xSdpa9inGbloJS8jI7I6WUtKRilj3eenQZozdWj9Y79BHGBwCHxg2gr9OYiveAridn9ru6Qz8-LZeLCq2tu-sA3U6mAz_aJsG-2_U-DBsbexQiESURBdKuQWuzsb_9sAngrEbWoZUOd4CupuAH0A6tdT90EF9nL1rdRXhzHM-z79dX3xbLfPXl5vPicpWbkpAxr7TkvMXQGlmRUldUtFDKArOWU90wIiihvK1ZXXCQgsjW6IKXjDRY6pqJmp1n-eHc-ADDVKsh2F6HnfLaqmPpZ5qBKiuMZZV48U9-CL45SU8ikQVNz0_mu4OZsF8TxFH1NhroOu3AT1FxIWXCRAL5ATTBxxig_duEYLWPW23VU9xqH7fCTKW4k3hx7DDVPTQn7ZhvAt4eAR2N7tqgnbHxxHEpaCFw4j4cOEg_f28hqGgsOAONDWBG1Xj7v7v8ATSLzmI</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Glaser, Beate</creator><creator>Schumacher, Johannes</creator><creator>Williams, Hywel J.</creator><creator>Jamra, Rami Abou</creator><creator>Ianakiev, Nikolai</creator><creator>Milev, Radoi</creator><creator>Ohlraun, Stephanie</creator><creator>Schulze, Thomas G.</creator><creator>Czerski, Piotr M.</creator><creator>Hauser, Joanna</creator><creator>Jönsson, Erick G.</creator><creator>Sedvall, Göran C.</creator><creator>Klopp, Norman</creator><creator>Illig, Thomas</creator><creator>Becker, Tim</creator><creator>Propping, Peter</creator><creator>Williams, Nigel M.</creator><creator>Cichon, Sven</creator><creator>Kirov, George</creator><creator>Rietschel, Marcella</creator><creator>Murphy, Kieran C.</creator><creator>O’Donovan, Michael C.</creator><creator>Nöthen, Markus M.</creator><creator>Owen, Michael J.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><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>ADTPV</scope><scope>AOWAS</scope></search><sort><creationdate>20050701</creationdate><title>No Association Between the Putative Functional ZDHHC8 Single Nucleotide Polymorphism rs175174 and Schizophrenia in Large European Samples</title><author>Glaser, Beate ; Schumacher, Johannes ; Williams, Hywel J. ; Jamra, Rami Abou ; Ianakiev, Nikolai ; Milev, Radoi ; Ohlraun, Stephanie ; Schulze, Thomas G. ; Czerski, Piotr M. ; Hauser, Joanna ; Jönsson, Erick G. ; Sedvall, Göran C. ; Klopp, Norman ; Illig, Thomas ; Becker, Tim ; Propping, Peter ; Williams, Nigel M. ; Cichon, Sven ; Kirov, George ; Rietschel, Marcella ; Murphy, Kieran C. ; O’Donovan, Michael C. ; Nöthen, Markus M. ; Owen, Michael J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-8a966f0efc9815a827fe59403f62ad3172126fb3b46e9719fca46531d09ab37b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Acyltransferases - genetics</topic><topic>Adult and adolescent clinical studies</topic><topic>Alleles</topic><topic>Association</topic><topic>Biological and medical sciences</topic><topic>Bulgaria - ethnology</topic><topic>Child</topic><topic>chromosome 22q11</topic><topic>Chromosomes, Human, Pair 22</topic><topic>disequilibrium</topic><topic>Female</topic><topic>Genetic Predisposition to Disease - genetics</topic><topic>Genetic Variation</topic><topic>Humans</topic><topic>linkage</topic><topic>Linkage Disequilibrium</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicin och hälsovetenskap</topic><topic>Membrane Proteins - genetics</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Risk Factors</topic><topic>Schizophrenia</topic><topic>Schizophrenia - enzymology</topic><topic>Schizophrenia - genetics</topic><topic>Sex Factors</topic><topic>VCFS</topic><topic>Whites - genetics</topic><topic>ZDHHC8</topic><topic>Zinc Fingers - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Glaser, Beate</creatorcontrib><creatorcontrib>Schumacher, Johannes</creatorcontrib><creatorcontrib>Williams, Hywel J.</creatorcontrib><creatorcontrib>Jamra, Rami Abou</creatorcontrib><creatorcontrib>Ianakiev, Nikolai</creatorcontrib><creatorcontrib>Milev, Radoi</creatorcontrib><creatorcontrib>Ohlraun, Stephanie</creatorcontrib><creatorcontrib>Schulze, Thomas G.</creatorcontrib><creatorcontrib>Czerski, Piotr M.</creatorcontrib><creatorcontrib>Hauser, Joanna</creatorcontrib><creatorcontrib>Jönsson, Erick G.</creatorcontrib><creatorcontrib>Sedvall, Göran C.</creatorcontrib><creatorcontrib>Klopp, Norman</creatorcontrib><creatorcontrib>Illig, Thomas</creatorcontrib><creatorcontrib>Becker, Tim</creatorcontrib><creatorcontrib>Propping, Peter</creatorcontrib><creatorcontrib>Williams, Nigel M.</creatorcontrib><creatorcontrib>Cichon, Sven</creatorcontrib><creatorcontrib>Kirov, George</creatorcontrib><creatorcontrib>Rietschel, Marcella</creatorcontrib><creatorcontrib>Murphy, Kieran C.</creatorcontrib><creatorcontrib>O’Donovan, Michael C.</creatorcontrib><creatorcontrib>Nöthen, Markus M.</creatorcontrib><creatorcontrib>Owen, Michael J.</creatorcontrib><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>SwePub</collection><collection>SwePub Articles</collection><jtitle>Biological psychiatry (1969)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Glaser, Beate</au><au>Schumacher, Johannes</au><au>Williams, Hywel J.</au><au>Jamra, Rami Abou</au><au>Ianakiev, Nikolai</au><au>Milev, Radoi</au><au>Ohlraun, Stephanie</au><au>Schulze, Thomas G.</au><au>Czerski, Piotr M.</au><au>Hauser, Joanna</au><au>Jönsson, Erick G.</au><au>Sedvall, Göran C.</au><au>Klopp, Norman</au><au>Illig, Thomas</au><au>Becker, Tim</au><au>Propping, Peter</au><au>Williams, Nigel M.</au><au>Cichon, Sven</au><au>Kirov, George</au><au>Rietschel, Marcella</au><au>Murphy, Kieran C.</au><au>O’Donovan, Michael C.</au><au>Nöthen, Markus M.</au><au>Owen, Michael J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>No Association Between the Putative Functional ZDHHC8 Single Nucleotide Polymorphism rs175174 and Schizophrenia in Large European Samples</atitle><jtitle>Biological psychiatry (1969)</jtitle><addtitle>Biol Psychiatry</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>58</volume><issue>1</issue><spage>78</spage><epage>80</epage><pages>78-80</pages><issn>0006-3223</issn><eissn>1873-2402</eissn><coden>BIPCBF</coden><abstract>It has been recently reported that a functional variant in the ZDHHC8 gene encoding a putative palmitoyltransferase directly confers susceptibility to schizophrenia in females (
Mukai et al 2004).
We investigated the putative risk allele (rs175174) in four schizophrenia association samples including a Bulgarian proband and parent sample (474 trios) and three case-control panels of European origin (1028 patients/1253 control subjects) in an attempt to replicate these findings.
Our results do not support the hypothesis that genetic variation at rs175174 is associated with increased risk for schizophrenia nor do they suggest the presence of gender-specific differences.
Our data suggest that the reported genetic association by
Mukai et al either represents type I error resulting from sampling variance or that rs175174 is in linkage disequilibrium (LD) with the functional variant for schizophrenia and different LD patterns obscure the detection of association.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>15992527</pmid><doi>10.1016/j.biopsych.2005.03.017</doi><tpages>3</tpages></addata></record> |
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subjects | Acyltransferases - genetics Adult and adolescent clinical studies Alleles Association Biological and medical sciences Bulgaria - ethnology Child chromosome 22q11 Chromosomes, Human, Pair 22 disequilibrium Female Genetic Predisposition to Disease - genetics Genetic Variation Humans linkage Linkage Disequilibrium Male Medical sciences Medicin och hälsovetenskap Membrane Proteins - genetics Polymorphism, Single Nucleotide - genetics Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychoses Reverse Transcriptase Polymerase Chain Reaction Risk Factors Schizophrenia Schizophrenia - enzymology Schizophrenia - genetics Sex Factors VCFS Whites - genetics ZDHHC8 Zinc Fingers - genetics |
title | No Association Between the Putative Functional ZDHHC8 Single Nucleotide Polymorphism rs175174 and Schizophrenia in Large European Samples |
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