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CONSENSUS TREATMENT RECOMMENDATIONS FOR LATE-ONSET POMPE DISEASE
INTRODUCTION: Pompe disease is a rare, autosomal recessive disorder caused by deficiency of the glycogen-degrading lysosomal enzyme acid alpha-glucosidase. Late-onset Pompe disease is a multisystem condition, with a heterogeneous clinical presentation that mimics other neuromuscular disorders. METHO...
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| Κύριοι συγγραφείς: | , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2011
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3534745/ https://ncbi.nlm.nih.gov/pubmed/22173792 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mus.22329 |
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