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...

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Detalles Bibliográficos
Autores principales: Lasa-Elgarresta, Jaione, Mosqueira-Martín, Laura, Naldaiz-Gastesi, Neia, Sáenz, Amets, López de Munain, Adolfo, Vallejo-Illarramendi, Ainara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770289/
https://www.ncbi.nlm.nih.gov/pubmed/31540302
http://dx.doi.org/10.3390/ijms20184548

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770289/
https://www.ncbi.nlm.nih.gov/pubmed/31540302
http://dx.doi.org/10.3390/ijms20184548

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