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NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease
Download from www.nature.comMutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect
Download from www.ncbi.nlm.nih.govBiochemical diagnosis of mitochondrial disorders
Download from link.springer.comNovel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies.
UploadAcyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I.
Download from doi.orgBaculovirus complementation restores a novelNDUFAF2mutation causing complex I deficiency
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