High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim

Am J Med Genet. 1999 Oct 29;86(5):499-500.
No abstract available

Publication types

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

MeSH terms

  • Chromosome Mapping
  • Connexin 26
  • Connexins / genetics*
  • Deafness / genetics*
  • Europe / ethnology
  • Genetic Carrier Screening
  • Genetic Markers
  • Humans
  • Israel
  • Jews / genetics*
  • Sequence Deletion*
  • Thymine

Substances

  • Connexins
  • GJB2 protein, human
  • Genetic Markers
  • Connexin 26
  • Thymine