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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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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | 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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