MITOCHONDRIAL DISEASES. “Mutations in the human mitochondrial ATP6 gene encoding ATP synthase subunit a/6…are at the base of neurodegenerative disorders like Neurogenic Ataxia and Retinitis Pigmentosa (NARP), Leigh syndrome (LS), Charcot–Marie–Tooth (CMT), and ataxia telangiectasia.”
https://lnkd.in/eEEix9C
linkedin post 2022-06-29 05:12:48
Nigel Fleming
September 21, 2022