Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy

This publication has 32 references indexed in Scilit:

• Replication and Transcription of Vertebrate Mitochondrial DNA
  Annual Review of Cell Biology, 1991
• 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 point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)
  Biochemical and Biophysical Research Communications, 1990
• A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
  Nature, 1990
• Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.
  Journal of Clinical Investigation, 1990
• Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation
  Cell, 1990
• Oxidative Phosphorylation Diseases
  Published by Springer Nature ,1990
• Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA
  Annals of Neurology, 1989
• Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
  New England Journal of Medicine, 1989
• Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
  Nature, 1988