Title : [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].

Pub. Date : 1999 Oct

PMID : 10514531






1 Functional Relationships(s)
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1 OBJECTIVE: To assess the frequency of the SCA1, SCA2,SCA3/MJD, SCA6, SCA7 and DRPLA CAG trinucleotide repeat expansions(CAG)n among individuals diagnosed with hereditary spinocerebellar ataxia(SCA) from Chinese families. trinucleotide atrophin 1 Homo sapiens