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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2011-1-25
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pubmed:abstractText |
Essential tremor (ET) is a complex genetic disorder for which no causative gene has been found. Recently, a genome-wide association study reported that two variants in the LINGO1 locus were associated to this disease. The aim of the present study was to test if this specific association could be replicated using a French-Canadian cohort of 259 ET patients and 479 ethnically matched controls. Our genotyping results lead us to conclude that no association exists between the key variant rs9652490 and ET (P(corr)?=?1.00).
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-11565522,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-12499305,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-17273975,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-17353225,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-17701901,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-19182806,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-19720553,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-19805735,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-20126254,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-20310002,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-20369371,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-20372186,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21264305-20600614
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1932-6203
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pubmed:author |
pubmed-author:BelouchiMajidM,
pubmed-author:BernardGenevièveG,
pubmed-author:BourassaCynthia VCV,
pubmed-author:ChouinardSylvainS,
pubmed-author:DiabSabrinaS,
pubmed-author:DionPatrick APA,
pubmed-author:DupréNicolasN,
pubmed-author:FournierHélèneH,
pubmed-author:PanissetMichelM,
pubmed-author:RaelsonJohnJ,
pubmed-author:RivièreJean-BaptisteJB,
pubmed-author:RouleauGuy AGA
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pubmed:issnType |
Electronic
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
e16254
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pubmed:meshHeading |
pubmed-meshheading:21264305-Canada,
pubmed-meshheading:21264305-Case-Control Studies,
pubmed-meshheading:21264305-Essential Tremor,
pubmed-meshheading:21264305-European Continental Ancestry Group,
pubmed-meshheading:21264305-Genetic Predisposition to Disease,
pubmed-meshheading:21264305-Genome-Wide Association Study,
pubmed-meshheading:21264305-Genotype,
pubmed-meshheading:21264305-Humans,
pubmed-meshheading:21264305-Membrane Proteins,
pubmed-meshheading:21264305-Nerve Tissue Proteins,
pubmed-meshheading:21264305-Polymorphism, Single Nucleotide
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pubmed:year |
2011
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pubmed:articleTitle |
LINGO1 variants in the French-Canadian population.
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pubmed:affiliation |
CHUM Research Center and the Department of Medicine, Université de Montréal, Montreal, Québec, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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