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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Detaylı Bibliyografya
Asıl Yazarlar: 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.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
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Article
Online Erişim: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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