## ~~ We studied a patient with a rnitochondrial encephalomyopathy characterized by the presence of all the cardinal features of both myoclonic epilepsy and ragged-red fibers (MERRF) and mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS) syndromes. Muscle biopsy show
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA
โ Scribed by R. W. Taylor; P. F. Chinnery; F. Haldane; A. A. M. Morris; L. A. Bindoff; Prof D. M. Turnbull; J. Wilson
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 430 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0364-5134
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