The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population

Clin Genet. 2004 Jun;65(6):506-8. doi: 10.1111/j.1399-0004.2004.00262.x.
No abstract available

Publication types

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

MeSH terms

  • Connexin 26
  • Connexins / genetics*
  • Ethnicity / genetics
  • Gene Frequency / genetics
  • Hearing Loss / ethnology*
  • Hearing Loss / genetics*
  • Humans
  • Mutation*
  • Sequence Deletion / genetics*

Substances

  • Connexins
  • GJB2 protein, human
  • Connexin 26