Maternally transmitted diabetes mellitus associated with the mitochondrial tRNALeu(UUR) A3243G mutation in a four-generation Han Chinese family

This publication has 21 references indexed in Scilit:

• A Mitochondrial Paradigm of Metabolic and Degenerative Diseases, Aging, and Cancer: A Dawn for Evolutionary Medicine
  Annual Review of Genetics, 2005
• Mitochondrial Genome Variation in Eastern Asia and the Peopling of Japan
  Genome Research, 2004
• Mitochondrial diabetes: Pathophysiology, clinical presentation, and genetic analysis
  American Journal of Medical Genetics, 2002
• The Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episode Syndrome-associated Human Mitochondrial tRNALeu(UUR) Mutation Causes Aminoacylation Deficiency and Concomitant Reduced Association of mRNA with Ribosomes
  Journal of Biological Chemistry, 2000
• Maternally inherited diabetes and deafness (MIDD): A distinct subtype of diabetes associated with a mitochondrial tRNALeu(UUR) gene point mutation
  Muscle & Nerve, 1995
• 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
• A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
  Nature, 1990
• Sequence and gene organization of mouse mitochondrial DNA
  Cell, 1981
• Sequence and organization of the human mitochondrial genome
  Nature, 1981