High-Resolution Genetic and Physical Mapping of Modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v)

This publication has 7 references indexed in Scilit:

• Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
  Nature Genetics, 2001
• Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
  Nature Genetics, 2001
• Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice
  Nature Genetics, 1998
• A First-Generation Whole Genome–Radiation Hybrid Map Spanning the Mouse Genome
  Genome Research, 1997
• A major gene affecting age-related hearing loss in C57BL/6J mice
  Hearing Research, 1997
• mdfw:A Deafness Susceptibility Locus That Interacts with Deaf Waddler (dfw)
  Genomics, 1997
• A high-resolution genetic map around waltzer on mouse Chromosome 10 and identification of a new allele of waltzer
  Mammalian Genome, 1997