Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor

Objective: Essential tremor (ET) is a common movement disorder that has a high heritability. A number of genetic studies have associated different genes and loci with ET, but few have investigated the biology of any of these genes. STK32B was significantly associated with ET in a large genome-wide a...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Liao, Calwing, Sarayloo, Faezeh, Vuokila, Veikko, Rochefort, Daniel, Akçimen, Fulya, Diamond, Simone, Houle, Gabrielle, Laporte, Alexandre D., Spiegelman, Dan, He, Qin, Catoire, Hélène, Dion, Patrick A., Rouleau, Guy A.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2020
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7413243/
https://ncbi.nlm.nih.gov/pubmed/32849812
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.00813
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