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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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Detalles Bibliográficos
Autores principales:	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.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer 2017
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281551/ https://www.ncbi.nlm.nih.gov/pubmed/30584593 http://dx.doi.org/10.1212/NXG.0000000000000195

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