Molecular genetics of the Pax gene family

Curr Opin Cell Biol. 1992 Dec;4(6):967-72. doi: 10.1016/0955-0674(92)90126-w.

Abstract

Three members of the Pax gene family are now known to be responsible for the established mouse developmental phenotypes Splotch, Small eye and undulated; two of these genes are implicated in the human congenital diseases Waardenburg's syndrome and aniridia. The mouse mutants will act as model systems for these human disorders and, in addition, will provide insights into the processes of vertebrate development.

Publication types

  • Review

MeSH terms

  • Animals
  • Drosophila / genetics*
  • Embryonic and Fetal Development / genetics
  • Humans
  • Mice
  • Multigene Family / genetics*
  • Mutation / genetics