CDH23

Материал из hpluswiki
Перейти к навигации Перейти к поиску

Cadherin-23 precursor (Otocadherin) [KIAA1774] [KIAA1812] [UNQ1894/PRO4340]

Publications[править]

Compound heterozygosity of the functionally null Cdh23(v-ngt) and hypomorphic Cdh23(ahl) alleles leads to early-onset progressive hearing loss in mice.


[Genetic factors in susceptibility to age- and noise-related hearing loss].


Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans.


Progressive hearing loss and increased susceptibility to noise-induced hearing loss in mice carrying a Cdh23 but not a Myo7a mutation.


Genetic influences in individual susceptibility to noise: a review.


Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss.