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Glycogen storage disease type III in Inuit children
GLYCOGEN STORAGE DISEASE TYPE III (GSD III) was diagnosed in 4 Inuit children (3 confirmed, 1 suspected case) at our institution over the last decade. This rare autosomal recessive disease, which results from a deficiency of the debranching enzyme required for complete degradation of the glycogen mo...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Canadian Medical Association
2005
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC545759/ https://ncbi.nlm.nih.gov/pubmed/15684118 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1503/cmaj.1031589 |
| Etiketak: |
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