Deletions of Xp provide evidence for the role of holocytochrome C-type synthase (HCCS) in congenital diaphragmatic hernia

Am J Med Genet A. 2010 Jun;152A(6):1588-90. doi: 10.1002/ajmg.a.33410.
No abstract available

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural

MeSH terms

  • Child
  • Chromosome Deletion*
  • Chromosomes, Human, X / genetics*
  • Hernia, Diaphragmatic / genetics*
  • Hernias, Diaphragmatic, Congenital*
  • Humans
  • Lyases / genetics*
  • Male

Substances

  • Lyases
  • cytochrome C synthetase