Atypical MELAS associated with mitochondrial tRNALys gene A8296G mutation

This publication has 13 references indexed in Scilit:

• The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS
  Annals of Neurology, 1999
• Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutation
  Neurology, 1997
• Bilateral Striatal Necrosis and MELAS Associated with a New T3308C Mutation in the Mitochondrial ND1 Gene
  Biochemical and Biophysical Research Communications, 1997
• Myoclonus epilepsy associated with ragged-red fibers: A G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNALys in two families
  Muscle & Nerve, 1997
• Optic neuropathy associated with mitochondrial tRNA^Leu(uur)A3243G mutation
  Ophthalmic Genetics, 1997
• Clinical features of melas and mitochondrial DNA mutations
  Muscle & Nerve, 1995
• A New Point Mutation at Nucleotide Pair-3291 of the Mitochondrial Transfer-RNALeu(Uur) Gene in a Patient with Mitochondrial Myopathy, Encephalopathy, Lactic-Acidosis, and Stroke-Like Episodes (MELAS)
  Biochemical and Biophysical Research Communications, 1994
• A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)
  Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1991
• A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
  Nature, 1990
• Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation
  Cell, 1990