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Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations
Limb-girdle muscular dystrophy recessive 1 (LGMDR1), previously known as LGMD2A, is a rare disease caused by mutations in the CAPN3 gene. It is characterized by progressive weakness of shoulder, pelvic, and proximal limb muscles that usually appears in children and young adults and results in loss o...
Kaydedildi:
| Yayımlandı: | Int J Mol Sci |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
MDPI
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6770289/ https://ncbi.nlm.nih.gov/pubmed/31540302 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20184548 |
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