Genotype-phenotype correlation of two prevalent GJB2 mutations in Chinese newborn infants ascertained from the Universal Newborn Hearing Screening Program

Am J Med Genet A. 2010 Nov;152A(11):2912-5. doi: 10.1002/ajmg.a.33698.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian People / genetics*
  • Auditory Threshold
  • China
  • Connexin 26
  • Connexins / genetics*
  • Genetic Association Studies*
  • Genotype
  • Hearing / genetics*
  • Hearing Loss / genetics
  • Hearing Loss / physiopathology
  • Humans
  • Infant, Newborn
  • Mutation / genetics*
  • Neonatal Screening*

Substances

  • Connexins
  • GJB2 protein, human
  • Connexin 26