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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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| Publicat a: | Front Physiol |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2018
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| Matèries: | |
| Accés en línia: | 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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