Molecular Genetics Overview of Primary Mitochondrial Myopathies

Mitochondrial disorders are the most common inherited conditions, characterized by defects in oxidative phosphorylation and caused by mutations in nuclear or mitochondrial genes. Due to its high energy request, skeletal muscle is typically involved. According to the International Workshop of Experts...

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Detalles Bibliográficos
Autores principales: Arena, Ignazio Giuseppe, Pugliese, Alessia, Volta, Sara, Toscano, Antonio, Musumeci, Olimpia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836969/
https://www.ncbi.nlm.nih.gov/pubmed/35160083
http://dx.doi.org/10.3390/jcm11030632

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836969/
https://www.ncbi.nlm.nih.gov/pubmed/35160083
http://dx.doi.org/10.3390/jcm11030632

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