The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)
- 1 December 1996
- journal article
- case report
- Published by Wiley in Muscle & Nerve
- Vol. 19 (12) , 1603-1604
- https://doi.org/10.1002/(sici)1097-4598(199612)19:12<1603::aid-mus10>3.0.co;2-s
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)The Lancet, 1991
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- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990
- Sequence and organization of the human mitochondrial genomeNature, 1981