Author:
Hirano Michio,Ricci Enzo,Richard Koenigsberger M.,Defendini Richard,Pavlakis Steven G.,DeVivo Darryl C.,DiMauro Salvatore,Rowland Lewis P.
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference61 articles.
1. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies;Goto;Nature,1990
2. Mitochondrial DNA mutation associated with Leber's hereditary optic atrophy;Wallace;Science,1988
3. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation;Shoffner;Cell,1990
4. Maternally inherited myopathy and cardiomyopathy associated with mutation in mitochondrial DNA tRNALeu(UUR);Zeviani;Lancet,1991
5. A new mitochondrial disease associated with mitochondrial DNA heteroplasmy;Holt;Am J Hum Genet,1990
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