Sensorineural hearing impairment non-syndromic, dominant DFNA11

Adv Otorhinolaryngol. 2000:56:103-6. doi: 10.1159/000059092.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 11*
  • Dyneins
  • Female
  • Genes, Dominant
  • Genetic Linkage
  • Genetic Markers
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Japan
  • Male
  • Myosin VIIa
  • Myosins / genetics*
  • Pedigree

Substances

  • Genetic Markers
  • MYO7A protein, human
  • Myosin VIIa
  • Myosins
  • Dyneins