Histochemical and molecular genetic study of MELAS and MERRF in Korean patients.
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episode (MELAS) and myoclonic epilepsy and ragged-red fibers (MERRF) are rare disorders caused by point mutation of the tRNA gene of the mitochondrial genome. To understand the pathogenetic mechanism of MELAS and MERRF, we studi...
| Main Authors: | , , , , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Korean Academy of Medical Sciences
2002
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054831/ |