Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.

Autosomal dominant cerebellar ataxia is a group of clinically and genetically heterogeneous disorders. We carried out genomewide linkage analysis in 15 families with autosomal dominant pure cerebellar ataxia (ADPCA). Evidence for linkage to chromosome 19p markers was found in nine families, and comb...

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Detalhes bibliográficos
Main Authors: Ishikawa, K, Tanaka, H, Saito, M, Ohkoshi, N, Fujita, T, Yoshizawa, K, Ikeuchi, T, Watanabe, M, Hayashi, A, Takiyama, Y, Nishizawa, M, Nakano, I, Matsubayashi, K, Miwa, M, Shoji, S, Kanazawa, I, Tsuji, S, Mizusawa, H
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715894/
https://ncbi.nlm.nih.gov/pubmed/9311738
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