Llwytho...
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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Int J Mol Sci |
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| Prif Awduron: | , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
MDPI
2019
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| Pynciau: | |
| Mynediad Ar-lein: | 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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