Pub. Date : 2016 Nov
PMID : 27686464
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
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 |