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Showing articles 0 to 2 of 2 Filter Applied: mitochondrial encephalomyopathy (Click to remove) Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature Mal Genet Genomic Med 10:e1955, Seed,L.M.,et al, 2022 A Young Man with Progressive Vision and Hearing Loss JAMA Neurol 73:880-883, Kung, N.H.,et al, 2016 Showing articles 0 to 2 of 2