Hereditary metabolic cardiomyopathies

Adv Pediatr. 1994:41:1-32.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Cardiomyopathy, Dilated / etiology
  • Cardiomyopathy, Dilated / genetics*
  • Cardiomyopathy, Dilated / metabolism
  • Child
  • Child, Preschool
  • DNA, Mitochondrial / genetics
  • Enzymes / deficiency
  • Glycogen Storage Disease / complications
  • Glycogen Storage Disease / genetics*
  • Glycogen Storage Disease / metabolism
  • Humans
  • Infant
  • Infant, Newborn
  • Lipid Metabolism, Inborn Errors / complications
  • Lipid Metabolism, Inborn Errors / genetics*
  • Lipid Metabolism, Inborn Errors / metabolism
  • Metabolism, Inborn Errors / complications
  • Metabolism, Inborn Errors / genetics
  • Metabolism, Inborn Errors / metabolism
  • Mitochondrial Myopathies / complications
  • Mitochondrial Myopathies / genetics
  • Mitochondrial Myopathies / metabolism
  • Mutation

Substances

  • DNA, Mitochondrial
  • Enzymes