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A guide to diagnosis and treatment of Leigh syndrome
Download from www.researchgate.netPLA2G6 gene mutations cause evolving spinocerebellar ataxia influenced by the genotype
Download from www.researchgate.netNUBPL mutations in patients with complex I deficiency and a distinct MRI pattern
Download from www.ncbi.nlm.nih.govA novel mutation in COQ2 leading to fatal infantile multisystem disease
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Download from repository.up.ac.zaA complex V ATP5A1 defect causes fatal neonatal mitochondrial encephalopathy
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Download from www.ncbi.nlm.nih.govCEP89 is required for mitochondrial metabolism and neuronal function in man and fly
Download from academic.oup.comRheumatoid Arthritis is a Lining Cell Disease: An Evolving Concept
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