Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice

This publication has 47 references indexed in Scilit:

• Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
  Human Molecular Genetics, 2001
• Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F
  American Journal of Human Genetics, 2001
• High-Resolution Genetic and Physical Mapping of Modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v)
  Genomics, 2001
• The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
  Nature Genetics, 2001
• Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
  Nature Genetics, 2001
• Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23
  American Journal of Human Genetics, 2001
• Genetic Heterogeneity of Usher Syndrome: Analysis of 151 Families with Usher Type I
  American Journal of Human Genetics, 2000
• Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer
  Hearing Research, 2000
• A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
  Nature Genetics, 2000
• Planar polarity: Out of joint?
  Current Biology, 2000