Is genotyping useful for the screening of medium-chain acyl-CoA dehydrogenase deficiency in France?

J Inherit Metab Dis. 1995;18(2):253-6. doi: 10.1007/BF00711781.
No abstract available

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyl-CoA Dehydrogenase
  • Acyl-CoA Dehydrogenases / deficiency*
  • Acyl-CoA Dehydrogenases / genetics
  • Alleles
  • France / epidemiology
  • Gene Frequency
  • Genotype*
  • Humans
  • Infant, Newborn
  • Lipid Metabolism, Inborn Errors / diagnosis*
  • Lipid Metabolism, Inborn Errors / epidemiology
  • Lipid Metabolism, Inborn Errors / genetics
  • Mass Screening*
  • Mutation
  • Sudden Infant Death / genetics

Substances

  • Acyl-CoA Dehydrogenases
  • Acyl-CoA Dehydrogenase