Carnitine-acylcarnitine translocase deficiency--a mild phenotype

J Inherit Metab Dis. 1997 Sep;20(5):714-5. doi: 10.1023/a:1005343013873.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Carnitine Acyltransferases / deficiency*
  • Humans
  • Infant
  • Male
  • Phenotype

Substances

  • Carnitine Acyltransferases