Clinical, neuropathological, and molecular study in two families with spinocerebellar ataxia type 6 (SCA6)

To clarify the clinical, neuropathological, and molecular characteristics of spinocerebellar ataxia type 6 (SCA6), two unrelated Japanese families with SCA6 were studied. A clinical feature of the two families was late onset "pure" cerebellar ataxia. Pathologically, three SCA6 brains consi...

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Bibliografski detalji
Glavni autori: Ishikawa, K, Watanabe, M, Yoshizawa, K, Fujita, T, Iwamoto, H, Yoshizawa, T, Harada, K, Nakamagoe, K, Komatsuzaki, Y, Satoh, A, Doi, M, Ogata, T, Kanazawa, I, Shoji, S, Mizusawa, H
Format: Artigo
Jezik:Inglês
Izdano: BMJ Group 1999
Teme:
Short Report
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1736420/
https://ncbi.nlm.nih.gov/pubmed/10369828
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