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Pompe disease: pathogenesis, molecular genetics and diagnosis
Pompe disease (PD) is a rare autosomal recessive disorder caused by mutations in the GAA gene, localized on chromosome 17 and encoding for acid alpha-1,4-glucosidase (GAA). Currently, more than 560 mutations spread throughout GAA gene have been reported. GAA catalyzes the hydrolysis of α-1,4 and α-1...
שמור ב:
הוצא לאור ב: | Aging (Albany NY) |
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Main Authors: | , , , , , , , , , , , , , |
פורמט: | Artigo |
שפה: | Inglês |
יצא לאור: |
Impact Journals
2020
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נושאים: | |
גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7467391/ https://ncbi.nlm.nih.gov/pubmed/32745073 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/aging.103794 |
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