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Polyglutamine spinocerebellar ataxias — from genes to potential treatments

The dominantly inherited spinocerebellar ataxias (SCAs) are a large and diverse group of neurodegenerative diseases. The most prevalent SCAs (SCA1, SCA2, SCA3, SCA6 and SCA7) are caused by expansion of a glutamine-encoding CAG repeat in the affected gene. These SCAs represent a substantial portion o...

詳細記述

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書誌詳細
出版年:Nat Rev Neurosci
主要な著者: Paulson, Henry L., Shakkottai, Vikram G., Brent Clark, H., Orr, Harry T.
フォーマット: Artigo
言語:Inglês
出版事項: 2017
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6420820/
https://ncbi.nlm.nih.gov/pubmed/28855740
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nrn.2017.92
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