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Noninvasive diagnosis of the MELAS syndrome from blood DNA

✍ Scribed by Joanna Poulton; Karl Morten

Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
101 KB
Volume
34
Category
Article
ISSN
0364-5134

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Sporadic MERRF/MELAS overlap syndrome as
Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNALeu(UUR) mutation of mitochondrial DNA
✍ Yolanda Campos; Miguel Angel Martin; Gustavo Lorenzo; Manuel Aparicio; Ana Cabel πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 378 KB πŸ‘ 1 views

## ~~ 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