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Mutations of CAPN3 in Korean Patients with Limb-Girdle Muscular Dystrophy
The limb-girdle muscular dystrophy type 2A (LGMD2A) is a recessively inherited disease caused by a mutation of the calpain 3 gene (CAPN3), and is considered one of the most prevalent subtypes of limb-girdle muscular dystrophy (LGMD). In this study, we aimed to identify CAPN3 mutations and to charact...
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| Main Authors: | , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
The Korean Academy of Medical Sciences
2007
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2693639/ https://ncbi.nlm.nih.gov/pubmed/17596655 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2007.22.3.463 |
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