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Variants in ATP5F1B are associated with dominantly inherited dystonia
UploadMyopathic mitochondrial DNA depletion syndrome associated with biallelic variants in LIG3
Download from academic.oup.comExploiting pyocyanin to treat mitochondrial disease due to respiratory complex III dysfunction
Download from www.nature.comImpaired complex I repair causes recessive Leber’s hereditary optic neuropathy
Download from doi.orgATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy
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