Mitochondria, mitophagy, and metabolic disease: towards assembling the puzzle

Dysregulation of the mitochondrial network in terminally differentiated cells contributes to a broad spectrum of disorders. Methylmalonic acidemia (MMA) is an autosomal recessive inborn error of intermediary metabolism caused by the deficiency of methylmalonyl-CoA mutase (MMUT) — a mitochondrial enz...

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Detalles Bibliográficos
Autores principales: Chen, Zhiyong, Berquez, Marine, Luciani, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2020
Materias:
Microreview
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278521/
https://www.ncbi.nlm.nih.gov/pubmed/32548571
http://dx.doi.org/10.15698/cst2020.06.222

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278521/
https://www.ncbi.nlm.nih.gov/pubmed/32548571
http://dx.doi.org/10.15698/cst2020.06.222

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