Title : RNAi prevents and reverses phenotypes induced by mutant human ataxin-1.

Pub. Date : 2016 Nov

PMID : 27686464






1 Functional Relationships(s)
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1 OBJECTIVE: Spinocerebellar ataxia type 1 is an autosomal dominant fatal neurodegenerative disease caused by a polyglutamine expansion in the coding region of ATXN1. polyglutamine ataxin 1 Homo sapiens