Title : [Molecular biology of polyglutamine diseases].

Pub. Date : 2002

PMID : 12661407






1 Functional Relationships(s)
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1 Polyglutamine diseases include at least 9 neurodegenerative disorders: Huntington"s disease (HD), dentatorubral pallidoluysian atrophy (DRPLA), spinobulbar muscular atrophy (SBMA), and spinocerebellar ataxia (SCA) type: 1-3, 6-7 and 17, each caused by a CAG-trinucleotide repeat expansion in a different gene. polyglutamine atrophin 1 Homo sapiens