Gene symbol: EFNB1. Disease: Craniofrontonasal syndrome

Hum Genet. 2008 Feb;123(1):105.
No abstract available

MeSH terms

  • Base Sequence
  • Ephrin-B1 / genetics*
  • Exons
  • Frameshift Mutation
  • Humans
  • Molecular Sequence Data
  • Nose / abnormalities*
  • Skull / abnormalities*
  • Syndrome

Substances

  • EFNB1 protein, human
  • Ephrin-B1

Associated data

  • GENBANK/HD070022