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Showing articles 0 to 2 of 2 Filter Applied: deafness (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 Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship J Pediatr 115:81-88, Sooth,F.A.,et al, 1989 Showing articles 0 to 2 of 2