Infantile encephalopathy associated with the MELAS A3243G mutation
Open Access
- 1 June 1999
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 134 (6) , 696-700
- https://doi.org/10.1016/s0022-3476(99)70283-0
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Cochlear origin of hearing loss in MELAS syndromeAnnals of Neurology, 1998
- Clinical features of melas and mitochondrial DNA mutationsMuscle & Nerve, 1995
- Mitochondrial encephalomyopathy: variable clinical expression within a single kindred.Journal of Neurology, Neurosurgery & Psychiatry, 1993
- Adult‐onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA Leu(UUR) mutationNeurology, 1993
- Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) geneFEBS Letters, 1993
- The Syndrome of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes Presenting Without StrokeArchives of Neurology, 1993
- Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNANeuromuscular Disorders, 1993
- Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafnessNature Genetics, 1992
- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990
- Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndromeAnnals of Neurology, 1984