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ATP Synthase Diseases of Mitochondrial Genetic Origin

Devastating human neuromuscular disorders have been associated to defects in the ATP synthase. This enzyme is found in the inner mitochondrial membrane and catalyzes the last step in oxidative phosphorylation, which provides aerobic eukaryotes with ATP. With the advent of structures of complete ATP...

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Detalhes bibliográficos
Publicado no:Front Physiol
Main Authors: Dautant, Alain, Meier, Thomas, Hahn, Alexander, Tribouillard-Tanvier, Déborah, di Rago, Jean-Paul, Kucharczyk, Roza
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5893901/
https://ncbi.nlm.nih.gov/pubmed/29670542
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2018.00329
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