Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa

N Engl J Med. 1998 Feb 19;338(8):548-50. doi: 10.1056/NEJM199802193380813.
No abstract available

Publication types

  • Letter

MeSH terms

  • Connexin 26
  • Connexins / genetics*
  • Genes, Recessive
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Lod Score
  • Point Mutation*

Substances

  • Connexins
  • Connexin 26