טוען...
Genotype-phenotype correlation in Pompe disease, a step forward
BACKGROUND: Pompe’s disease is a progressive myopathy caused by mutations in the lysosomal enzyme acid alphaglucosidase gene (GAA). A wide clinical variability occurs also in patients sharing the same GAA mutations, even within the same family. METHODS: For a large series of GSDII patients we collec...
שמור ב:
| הוצא לאור ב: | Orphanet J Rare Dis |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2014
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4249737/ https://ncbi.nlm.nih.gov/pubmed/25103075 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-014-0102-z |
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