Noninvasive diagnosis of the MELAS syndrome from blood DNA
- 1 July 1993
- journal article
- letter
- Published by Wiley in Annals of Neurology
- Vol. 34 (1) , 116
- https://doi.org/10.1002/ana.410340124
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- MELAS: Clinical features, biochemistry, and molecular geneticsAnnals of Neurology, 1992
- Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS)Neurology, 1992
- Mitochondrial encephalopathies: molecular genetic diagnosis from blood samplesThe Lancet, 1991
- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990