Molecular mechanism of a frequent genetic form of deafness

N Engl J Med. 2003 Aug 14;349(7):716-7. doi: 10.1056/NEJMc030327.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Animals
  • Chromosomes, Human, Pair 13
  • Chromosomes, Mammalian
  • Connexin 26
  • Connexin 30
  • Connexins / genetics*
  • Deafness / genetics*
  • Heterozygote
  • Humans
  • Mice
  • Mice, Knockout
  • Sequence Deletion

Substances

  • Connexin 30
  • Connexins
  • GJB6 protein, human
  • Gjb6 protein, mouse
  • Connexin 26