Treating genetic diseases: lessons from three children

Pediatr Res. 1990 Jun;27(6 Suppl):S10-6. doi: 10.1203/00006450-199006001-00004.
No abstract available

Publication types

  • Case Reports
  • Review

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / therapy
  • Ammonia / blood
  • Child
  • Genetic Diseases, Inborn / therapy*
  • Genetic Therapy
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Methylmalonic Acid / urine
  • Ornithine Carbamoyltransferase Deficiency Disease
  • Transplantation

Substances

  • Ammonia
  • Methylmalonic Acid