The myoclonic epilepsy and ragged-red fiber mutation provides new insights into human mitochondrial function and genetics

Am J Hum Genet. 1998 Apr;62(4):745-51. doi: 10.1086/301813.
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • DNA, Mitochondrial*
  • Genome, Human
  • Humans
  • MERRF Syndrome / genetics*
  • MERRF Syndrome / pathology
  • Mitochondria / genetics*
  • Mitochondria / pathology
  • Mutation*

Substances

  • DNA, Mitochondrial