Is the medium-chain acyl-CoA dehydrogenase G985 mutation involved in sudden infant death in Norway?

This publication has 8 references indexed in Scilit:

• The frequency of a disease‐causing point mutation in the gene coding for medium‐chain acyl‐CoA dehydrogenase in sudden infant death syndrome
  Acta Paediatrica, 1993
• Prevalence of medium-chain acyl-coenzyme A dehydrogenase deficiency in the sudden infant death syndrome
  The Journal of Pediatrics, 1993
• Frequency of Medium-Chain Acyl-CoA Dehydrogenase Deficiency G-985 Mutation in Sudden Infant Death Syndrome
  Pediatric Research, 1992
• [Medium chain acyl-CoA dehydrogenase (MCAD) deficiency: a life-threatening defect of fatty acid oxidation].
  1992
• Medium chain acyl-CoA dehydrogenase deficiency in the United Kingdom.
  1992
• Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli
  Human Genetics, 1991
• Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency
  Biochemical and Biophysical Research Communications, 1990
• Sudden infant death and inherited disorders of fat oxidation.
  1986