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Role of Mitochondrial Dysfunction in the Pathogenesis of Huntington’s Disease

Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder that is caused by a pathological expansion of CAG repeats within the gene encoding for a 350 kD protein called huntingtin. This polyglutamine expansion within huntingtin is the causative factor in the pathogenesis of HD, h...

詳細記述

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書誌詳細
主要な著者: Quintanilla, Rodrigo A., Johnson, Gail V.W.
フォーマット: Artigo
言語:Inglês
出版事項: 2009
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2757461/
https://ncbi.nlm.nih.gov/pubmed/19622387
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainresbull.2009.07.010
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