Title : Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17.

Pub. Date : 2008 Feb

PMID : 18043721






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 SCA17 is a typical polyglutamine disease caused by CAG repeat expansion in TBP (TATA binding protein), and is unique in that the pure expanded polyglutamine tract is coded by either a simple configuration with long stretches of pure CAGs or a complex configuration containing CAA interruptions. polyglutamine ataxin 7 Homo sapiens