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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2017
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Materias: | |
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 |