| Literature DB >> 9605731 |
K G Kimata1, L Gordan, E T Ajax, P H Davis, T Grabowski.
Abstract
We describe a 60-year-old man with MELAS syndrome (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes) and discuss the mitochondrial DNA point mutation 3243. A diagnosis of MELAS should be considered in the appropriate clinical setting at any age.Entities:
Mesh：
Year: 1998 PMID： 9605731 DOI： 10.1001/archneur.55.5.722
Source DB: PubMed Journal: Arch Neurol ISSN： 0003-9942