Spectrum of GJB2 gene variants in Indian children with non-syndromic hearing loss

Indian J Med Res. 2018 Jun;147(6):615-618. doi: 10.4103/ijmr.IJMR_76_16.
No abstract available

Publication types

  • Letter

MeSH terms

  • Asian People
  • Child
  • Connexin 26
  • Connexins / genetics*
  • Hearing Loss / genetics*
  • Humans
  • India
  • Mutation

Substances

  • Connexins
  • GJB2 protein, human
  • Connexin 26