Title : Ataxin-2 and huntingtin interact with endophilin-A complexes to function in plastin-associated pathways.

Pub. Date : 2005 Oct 1

PMID : 16115810






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Spinocerebellar ataxia type 2 is an inherited neurodegenerative disorder that is caused by an expanded trinucleotide repeat in the SCA2 gene, encoding a polyglutamine stretch in the gene product ataxin-2. polyglutamine ataxin 2 Homo sapiens