Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13

Adv Otorhinolaryngol. 2000:56:84-96. doi: 10.1159/000059085.
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Chromosome Mapping*
  • Chromosomes, Human*
  • Genes, Dominant
  • Genetic Linkage
  • Genetic Markers
  • Hearing Loss, Sensorineural / genetics*
  • Hearing Loss, Sensorineural / physiopathology
  • Humans

Substances

  • Genetic Markers