Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndrome

This publication has 9 references indexed in Scilit:

• The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in Japan.
  Journal of Clinical Endocrinology & Metabolism, 1994
• Are duplications of mitochondrial DNA characteristic of Kearns—Sayre syndrome?
  Human Molecular Genetics, 1994
• A Subtype of Diabetes Mellitus Associated with a Mutation of Mitochondrial DNA
  New England Journal of Medicine, 1994
• Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetics
  The Lancet, 1993
• Fetal growth and impaired glucose tolerance in men and women
  Diabetologia, 1993
• Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form
  Human Molecular Genetics, 1993
• The expanding clinical spectrum of mitochondrial diseases
  Brain & Development, 1993
• Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
  Nature Genetics, 1992
• Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion
  Nature Genetics, 1992