MUTATIONS OF ATP SYNTHASE. “The majority of mutations in the ATP synthase that are associated with disease are located in the mitochondrial ATP6 gene, which encodes subunit-a. This is likely reflective of the importance of subunit-a in the proton translocation.”
https://lnkd.in/ed8KNUV
linkedin post 2022-06-29 05:12:48
Nigel Fleming
September 21, 2022