Mitochondrial DNA mutation in a Chinese family with myoclonic epilepsy and ragged-red fiber disease
- 14 February 1991
- journal article
- case report
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 174 (3) , 1109-1116
- https://doi.org/10.1016/0006-291x(91)91535-k
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
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- Sequence and organization of the human mitochondrial genomeNature, 1981
- Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities): Disease entity or a syndrome?Journal of the Neurological Sciences, 1980