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Compound Heterozygosity of the Functionally Null Cdh23(v-ngt) and Hypomorphic Cdh23(ahl) Alleles Leads to Early-onset Progressive Hearing Loss in Mice
The waltzer (v) mouse mutant harbors a mutation in Cadherin 23 (Cdh23) and is a model for Usher syndrome type 1D, which is characterized by congenital deafness, vestibular dysfunction, and prepubertal onset of progressive retinitis pigmentosa. In mice, functionally null Cdh23 mutations affect stereo...
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| Główni autorzy: | , , , , , , , , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
Japanese Association for Laboratory Animal Science
2013
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4160959/ https://ncbi.nlm.nih.gov/pubmed/24172198 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1538/expanim.62.333 |
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