No rare deleterious variants from STK32B, PPARGC1A, and CTNNA3 are associated with essential tremor

OBJECTIVE: To assess the contribution of variants in STK32B, PPARGC1A, and CTNNA3 as essential tremor (ET) predisposing factors following their association in a 2-stage genome-wide association study (GWAS). METHODS: The coding regions of these genes was examined for the presence of rare variants usi...

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保存先:
書誌詳細
出版年:Neurol Genet
主要な著者: Houle, Gabrielle, Ambalavanan, Amirthagowri, Schmouth, Jean-François, Leblond, Claire S., Spiegelman, Dan, Laurent, Sandra B., Bourassa, Cynthia V., Grayson, Celene, Panisset, Michel, Chouinard, Sylvain, Dupré, Nicolas, Vilariño-Güell, Carles, Rajput, Alex, Girard, Simon L., Dion, Patrick A., Rouleau, Guy A.
フォーマット: Artigo
言語:Inglês
出版事項: Wolters Kluwer 2017
主題:
Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6281551/
https://ncbi.nlm.nih.gov/pubmed/30584593
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000195
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