A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation

J Med Genet. 2001 Jan;38(1):61-5. doi: 10.1136/jmg.38.1.61.
No abstract available

Publication types

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

MeSH terms

  • Alleles
  • Amino Acid Substitution
  • Belgium
  • Chromosomes, Artificial, Yeast
  • Chromosomes, Human, Pair 14 / genetics
  • Cochlear Diseases / genetics
  • Contig Mapping
  • Extracellular Matrix Proteins
  • Family Health
  • Female
  • Gene Frequency
  • Haplotypes
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Male
  • Microsatellite Repeats
  • Netherlands
  • Point Mutation
  • Proteins / genetics*
  • Vestibular Diseases / genetics

Substances

  • COCH protein, human
  • Extracellular Matrix Proteins
  • Proteins