Title : Spinocerebellar ataxia type 2 (SCA2): clinical features and genetic analysis.

Pub. Date : 2008 Oct

PMID : 18499737






2 Functional Relationships(s)
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Compound Name
Protein Name
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1 Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant neurodegenerative disease that results from the expansion of an unstable trinucleotide CAG repeat encoding for a polyglutamine tract. polyglutamine ataxin 2 Homo sapiens
2 Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant neurodegenerative disease that results from the expansion of an unstable trinucleotide CAG repeat encoding for a polyglutamine tract. polyglutamine ataxin 2 Homo sapiens