Concepedia
Hearing Research · 2006 · 18 citations · 15 references
Open access
Life SciencesMolecular BiologyMolecular GeneticsMolecular EvolutionDevelopmental MutationsEmbryonic Lethal MutationsGenetic DisordersMutation ProcessesMutationSpontaneous Mutation Rates
15
Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses
Qing Yin Zheng, Kenneth R. Johnson, Lawrence C. Erway · Hearing Research · 1999 · 842 citations
Health Professions, Audiology, Auditory Electrophysiology +12
Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F
Zubair M. Ahmed, Saima Riazuddin, Steven L. Bernstein et al. · The American Journal of Human Genetics · 2001 · 414 citations · Full text
Life Sciences, Genetics, Molecular Genetics +6
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
Kumar N. Alagramam, Crystal L. Murcia, Heajoon Y. Kwon et al. · Nature Genetics · 2001 · 315 citations
Medicine, Genetics, Molecular Genetics +13
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23
Zubair M. Ahmed · Human Molecular Genetics · 2003 · 294 citations · Full text
Medicine, Genetics, Molecular Genetics +17
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
Kumar N. Alagramam · Human Molecular Genetics · 2001 · 285 citations · Full text
Life Sciences, Genetics, Molecular Genetics +10