The Pathogenic Role of Point Mutations Affecting the Translational Initiation Codon of Mitochondrial Genes

This publication has 11 references indexed in Scilit:

• About the “Pathological” Role of the mtDNA T3308C Mutation…
  American Journal of Human Genetics, 1999
• A Stop-Codon Mutation in the Human mtDNA Cytochrome c Oxidase I Gene Disrupts the Functional Structure of Complex IV
  American Journal of Human Genetics, 1999
• Revolution in mitochondrial medicine
  FEBS Letters, 1999
• An mtDNA Mutation in the Initiation Codon of the Cytochrome C Oxidase Subunit II Gene Results in Lower Levels of the Protein and a Mitochondrial Encephalomyopathy
  American Journal of Human Genetics, 1999
• Somatic mutations of the mitochondrial genome in human colorectal tumours
  Nature Genetics, 1998
• Mitochondria in neuromuscular disorders
  Biochimica et Biophysica Acta (BBA) - Bioenergetics, 1998
• Mitochondrial Disorders
  Medicine, 1998
• Bilateral Striatal Necrosis and MELAS Associated with a New T3308C Mutation in the Mitochondrial ND1 Gene
  Biochemical and Biophysical Research Communications, 1997
• MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNALys and premature translation termination
  Nature Genetics, 1995
• Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNALeu(UUR) gene
  Muscle & Nerve, 1995