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Novel Mutation m.10372A>G in MT-ND3 Causing Sensorimotor Axonal Polyneuropathy
Download from doi.orgSQSTM1/p62-Directed Metabolic Reprogramming Is Essential for Normal Neurodifferentiation
Download from doi.orgIntra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26
Download from www.ncbi.nlm.nih.govCyclophilin D, a target for counteracting skeletal muscle dysfunction in mitochondrial myopathy
Download from europepmc.orgRescue of primary ubiquinone deficiency due to a novelCOQ7defect using 2,4–dihydroxybensoic acid
Download from www.ncbi.nlm.nih.govComplete Deletion of a POLG1 Allele in a Patient with Alpers Syndrome
Download from www.ncbi.nlm.nih.govBaculovirus complementation restores a novelNDUFAF2mutation causing complex I deficiency
Download from www.researchgate.netMtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome
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