Article
SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family.
Annals of neurology - 1 Jan 2001
Fujigasaki H, Verma I C, Camuzat A, Margolis R L, Zander C, Lebre A S, Jamot L, Saxena R, Anand I, Holmes S E, Ross C A, Dürr A, Brice A
Abstract excerpt
Spinocerebellar ataxia 12 (SCA12) is an autosomal dominant cerebellar ataxia (ADCA) described in a single family with a CAG repeat expansion in the PPP2R2B gene. We screened 247 index cases, including 145 families with ADCA, for this expansion. An expanded repeat ranging from 55 to 61 triplets was detected in 6 affected and 3 unaffected individuals at risk in a single family from India. The association of the...
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