Clue to a new deafness gene: a large Chinese nonsyndromic hearing loss family linked to DFNA4

J Genet Genomics. 2012 Dec 20;39(12):653-7. doi: 10.1016/j.jgg.2012.11.002. Epub 2012 Nov 16.
No abstract available

Publication types

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

MeSH terms

  • Asian People / genetics
  • China
  • Chromosome Mapping
  • Chromosomes, Human, Pair 19 / genetics
  • DNA Mutational Analysis
  • Deafness / ethnology
  • Deafness / genetics*
  • Family Health
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Hearing Loss, Sensorineural / ethnology
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Male
  • Myosin Heavy Chains / genetics*
  • Myosin Type II / genetics*
  • Pedigree

Substances

  • MYH14 protein, human
  • Myosin Type II
  • Myosin Heavy Chains

Supplementary concepts

  • Nonsyndromic sensorineural hearing loss