Author:
Moraes Carlos T.,Ciacci Federica,Silvestri Gabriella,Shanske Sara,Sciacco Monica,Hirano Michio,Schon Eric A.,Bonilla Eduardo,DiMauro Salvatore
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference36 articles.
1. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: a distinctive clinical syndrome;Pavlakis;Ann Neurol,1984
2. MELAS: an original case and clinical criteria for diagnosis;Hirano;Neuromusc Disord,1992
3. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies;Goto;Nature,1990
4. A point mutation in the mitochondrial tRNALeu(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes);Kobayashi;Biochem Biophys Res Commun,1990
5. Mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes (MELAS): a correlative study on clinical features and mitochondrial DNA mutation;Goto;Neurology,1992
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