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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...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2008
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| Θέματα: | |
| Διαθέσιμο Online: | 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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