Mitochondrial biology and dysfunction in secondary mitochondrial disease

Mitochondrial diseases are a broad, genetically heterogeneous class of metabolic disorders characterized by deficits in oxidative phosphorylation (OXPHOS). Primary mitochondrial disease (PMD) defines pathologies resulting from mutation of mitochondrial DNA (mtDNA) or nuclear genes affecting either m...

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Detalles Bibliográficos
Autores principales: Baker, Megan J., Crameri, Jordan J., Thorburn, David R., Frazier, Ann E., Stojanovski, Diana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727669/
https://www.ncbi.nlm.nih.gov/pubmed/36475414
http://dx.doi.org/10.1098/rsob.220274

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727669/
https://www.ncbi.nlm.nih.gov/pubmed/36475414
http://dx.doi.org/10.1098/rsob.220274

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