Temporal Neuropathological and Behavioral Phenotype of 6(Neo)/6(Neo) Pompe Disease Mice

Pompe disease (glycogen storage disease II) is caused by mutations in the acid α-glucosidase gene. The most common form is rapidly progressive with glycogen storage, particularly in muscle, that leads to profound weakness, cardiac failure, and death by the age of two years. Although usually consider...

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書誌詳細
主要な著者: Sidman, Richard L., Taksir, Tatyana, Fidler, Jonathan, Zhao, Michael, Dodge, James C., Passini, Marco A., Raben, Nina, Thurberg, Beth L., Cheng, Seng H., Shihabuddin, Lamya S.
フォーマット: Artigo
言語:Inglês
出版事項: 2008
主題:
Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2743262/
https://ncbi.nlm.nih.gov/pubmed/18648322
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/NEN.0b013e3181815994
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