Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and diabetes mellitus: molecular genetic analysis and family study

This publication has 22 references indexed in Scilit:

• MELAS: Clinical features, biochemistry, and molecular genetics
  Annals of Neurology, 1992
• Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion
  Nature Genetics, 1992
• A specific point mutation in the mitochondrial genome of Caucasians with MELAS
  Human Genetics, 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
• Widespread tissue distribution of a tRNA ^Leu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome
  Neurology, 1991
• Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples
  The Lancet, 1991
• A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
  Nature, 1990
• Kearns‐Sayre syndrome presenting as renal tubular acidosis
  Neurology, 1990
• Mitochondrial myopathies
  Annals of Neurology, 1985
• Mitochondrial Inheritance in a Mitochondrially Mediated Disease
  New England Journal of Medicine, 1983