R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease?

Eur J Hum Genet. 2001 Jan;9(1):70. doi: 10.1038/sj.ejhg.5200569.
No abstract available

Publication types

  • Comment
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Connexins / genetics*
  • Deafness / genetics
  • Family Health
  • Female
  • Humans
  • Male
  • Mutation
  • Polymorphism, Genetic
  • Skin Diseases / genetics

Substances

  • Connexins
  • GJB3 protein, human