Molecular and Clinical Correlations in Spinocerebellar Ataxia Type I: Evidence for Familial Effects on the Age at Onset

The spinocerebellar ataxias are a group of debilitating neurodegenerative diseases for which a clinical classification system has proved unreliable. We have recently isolated the gene for spinocerebellar ataxia type 1 (SCA1) and have shown that the disease is caused by an expanded, unstable, CAG tri...

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Detalhes bibliográficos
Main Authors: Ranum, Laura P. W., Chung, Ming-Yi, Banfi, Sandro, Bryer, Alan, Schut, Lawrence J., Ramesar, Raj, Duvick, Lisa A., McCall, Alanna, Subramony, S. H., Goldfarb, Lev, Gomez, Christopher, Sandkuijl, Lodewijk A., Orr, Harry T., Zoghbi, Huda Y.
Formato: Artigo
Idioma:Inglês
Publicado em: 1994
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1918367/
https://ncbi.nlm.nih.gov/pubmed/8037204
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