Barth syndrome may be due to an acyltransferase deficiency

Curr Biol. 1997 Aug 1;7(8):R465-6. doi: 10.1016/s0960-9822(06)00237-5.
No abstract available

Publication types

  • Letter

MeSH terms

  • Acyltransferases / deficiency*
  • Acyltransferases / genetics*
  • Amino Acid Sequence
  • Cardiomyopathies / enzymology*
  • Cardiomyopathies / genetics*
  • Genetic Linkage
  • Growth Disorders / enzymology
  • Growth Disorders / genetics
  • Humans
  • Male
  • Mitochondrial Myopathies / enzymology
  • Mitochondrial Myopathies / genetics
  • Molecular Sequence Data
  • Mutation
  • Sequence Homology, Amino Acid
  • Syndrome
  • X Chromosome / genetics

Substances

  • Acyltransferases