## ~~ 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
Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNALeu(UUR) gene
β Scribed by Dr. Yasutoshi Koga; Dr. Mercy Davidson; Dr. Eric A. Schon; Dr. Michael P. King
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 458 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0148-639X
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