Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype

Mitochondrial dysfunction is considered the major contributor to skeletal muscle wasting in different conditions. Genetically determined neuromuscular disorders occur as a result of mutations in the structural proteins of striated muscle cells and therefore are often combined with cardiac phenotype,...

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Detalles Bibliográficos
Autores principales: Ignatieva, Elena, Smolina, Natalia, Kostareva, Anna, Dmitrieva, Renata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8307986/
https://www.ncbi.nlm.nih.gov/pubmed/34298968
http://dx.doi.org/10.3390/ijms22147349

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8307986/
https://www.ncbi.nlm.nih.gov/pubmed/34298968
http://dx.doi.org/10.3390/ijms22147349

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