No association between DFNA6 and Pro250Arg mutation in FGFR3

Am J Med Genet. 1999 Oct 15;88(5):451.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Age of Onset
  • Child
  • Child, Preschool
  • Chromosomes, Human, Pair 4
  • Genetic Linkage*
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Point Mutation*
  • Protein-Tyrosine Kinases*
  • Receptor, Fibroblast Growth Factor, Type 3
  • Receptors, Fibroblast Growth Factor / genetics*

Substances

  • Receptors, Fibroblast Growth Factor
  • FGFR3 protein, human
  • Protein-Tyrosine Kinases
  • Receptor, Fibroblast Growth Factor, Type 3