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4. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype. Kanaumi T; Hirose S; Goto Y; Naitou E; Mitsudome A Pediatr Neurol; 2006 Mar; 34(3):235-8. PubMed ID: 16504796 [TBL] [Abstract][Full Text] [Related]
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