GJB2 gene mutations in Slovak hearing-impaired patients of Caucasian origin: spectrum, frequencies and SNP analysis

Clin Genet. 2005 Dec;68(6):554-7. doi: 10.1111/j.1399-0004.2005.00529.x.
No abstract available

Publication types

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

MeSH terms

  • Connexin 26
  • Connexins / genetics*
  • DNA Primers
  • Genetic Predisposition to Disease*
  • Genetic Testing
  • Haplotypes / genetics
  • Hearing Loss / epidemiology*
  • Hearing Loss / genetics*
  • Humans
  • Mutation / genetics*
  • Polymorphism, Single Nucleotide / genetics
  • Sequence Analysis, DNA
  • Slovakia / epidemiology
  • White People / genetics

Substances

  • Connexins
  • DNA Primers
  • GJB2 protein, human
  • Connexin 26