Yüklüyor......

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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Front Physiol
Asıl Yazarlar: Dautant, Alain, Meier, Thomas, Hahn, Alexander, Tribouillard-Tanvier, Déborah, di Rago, Jean-Paul, Kucharczyk, Roza
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2018
Konular:
Online Erişim: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
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!