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Neurology ; 57(8): 1502-4, 2001 Oct 23.
Article in English | MEDLINE | ID: mdl-11673601

ABSTRACT

SCA6 is caused by CAG expansion in the alpha 1A voltage-dependent calcium channel subunit gene. The authors studied an Italian family in which one patient carried a fully expanded SCA6 allele with 26-CAG repeats, whereas the other affected family member was homozygous for an intermediate-size allele of 19-CAG repeats. Three family members, heterozygous for the intermediate allele, were clinically unaffected. The findings demonstrate a dose-dependent pathogenic effect of an intermediate CAG expansion in the SCA6 gene.


Subject(s)
Calcium Channels/genetics , Cerebellar Ataxia/genetics , Trinucleotide Repeat Expansion , Adult , Family Health , Female , Homozygote , Humans , Male , Pedigree
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