MPV17 Mutations Are Associated With a Quiescent Energetic Metabolic Profile

Mutations in the MPV17 gene are associated with hepatocerebral form of mitochondrial depletion syndrome. The mechanisms through which MPV17 mutations cause respiratory chain dysfunction and mtDNA depletion is still unclear. The MPV17 gene encodes an inner membrane mitochondrial protein that was rece...

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Detalles Bibliográficos
Autores principales: Jacinto, Sandra, Guerreiro, Patrícia, de Oliveira, Rita Machado, Cunha-Oliveira, Teresa, Santos, Maria João, Grazina, Manuela, Rego, Ana Cristina, Outeiro, Tiago F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cellular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8011494/
https://www.ncbi.nlm.nih.gov/pubmed/33815063
http://dx.doi.org/10.3389/fncel.2021.641264

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8011494/
https://www.ncbi.nlm.nih.gov/pubmed/33815063
http://dx.doi.org/10.3389/fncel.2021.641264

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