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Clinical Analysis of Algerian Patients with Pompe Disease
Pompe's disease is a metabolic myopathy caused by a deficiency of acid alpha-glucosidase (GAA), also called acid maltase, an enzyme that degrades lysosomal glycogen. The clinical presentation of Pompe's disease is variable with respect to the age of onset and rate of disease progression. P...
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| Publicado no: | J Neurodegener Dis |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi Publishing Corporation
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5317144/ https://ncbi.nlm.nih.gov/pubmed/28265479 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/9427269 |
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