DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment

Clin Genet. 2011 Jun;79(6):594-8. doi: 10.1111/j.1399-0004.2010.01593.x.
No abstract available

Publication types

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

MeSH terms

  • Chromosomes, Human, Pair 11 / genetics*
  • Female
  • Genes, Recessive*
  • Genetic Loci*
  • Genome-Wide Association Study
  • Haplotypes
  • Hearing Loss / genetics*
  • Humans
  • Male
  • Pedigree
  • Sequence Analysis, DNA