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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Miyasaka, Yuki, Suzuki, Sari, Ohshiba, Yasuhiro, Watanabe, Kei, Sagara, Yoshihiko, Yasuda, Shumpei P., Matsuoka, Kunie, Shitara, Hiroshi, Yonekawa, Hiromichi, Kominami, Ryo, Kikkawa, Yoshiaki
Format: Artigo
Idioma:Inglês
Publicat: Japanese Association for Laboratory Animal Science 2013
Matèries:
Original
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars