GJB2 and hearing impairment: promoter defects do not explain the excess of monoallelic mutations

J Med Genet. 2008 Sep;45(9):607-8. doi: 10.1136/jmg.2008.059873.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Alleles*
  • Connexin 26
  • Connexins / genetics*
  • Hearing Disorders / genetics*
  • Humans
  • Mutation*
  • Promoter Regions, Genetic*

Substances

  • Connexins
  • GJB2 protein, human
  • Connexin 26