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Molecular Genetic Diagnosis in Korean Patients with Myoclonic Epilepsy with Ragged Red Fiber (MERRF) Syndrome

Ko TS, Lee SA, Choe G, Yoo HW

  • KMID: 1561831
  • J Korean Pediatr Soc.
  • 1998 Jul;41(7):941-952.
PURPOSE: Myoclonic epilepsy with ragged red fiber (MERRF) syndrome is a disease of the mitochondrial encephalomyopathies, characterized by progressive myoclonus (action), epilepsy, cerebellar ataxia, intention tremor, muscle weakness, progressive dementia,...
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