| Literature DB >> 18590963 |
Rita Horváth1, Ralf Reilmann, Elke Holinski-Feder, E Bernd Ringelstein, Thomas Klopstock.
Abstract
While Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes (MELAS) is typically associated with mutations in the mitochondrial tRNA(Leu) gene, mutations in complex I subunit genes of the mtDNA have emerged as a second significant cause. Here we report a novel mutation in the mitochondrial complex I subunit gene ND1 in a patient with late-onset MELAS. The 3380G>A mutation shows very good evidence of pathogenicity as it is heteroplasmic, undetectable in controls, alters a highly conserved amino acid, and is more abundant in ragged-red than in normal muscle fibers. These findings support the significant role of complex I mutations in MELAS.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18590963 DOI: 10.1016/j.nmd.2008.05.002
Source DB: PubMed Journal: Neuromuscul Disord ISSN: 0960-8966 Impact factor: 4.296