An ENU-Induced Mutation of Cdh23 Causes Congenital Hearing Loss, but No Vestibular Dysfunction, in Mice

Mutations in the human cadherin 23 (CDH23) gene cause deafness, neurosensory, autosomal recessive 12 (DFNB12) nonsyndromic hearing loss or Usher syndrome, type 1D (characterized by hearing impairment, vestibular dysfunction, and visual impairment). Reported waltzer mouse strains each harbor a Cdh23-...

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Detaylı Bibliyografya
Asıl Yazarlar: Manji, Shehnaaz S.M., Miller, Kerry A., Williams, Louise H., Andreasen, Lotte, Siboe, Maria, Rose, Elizabeth, Bahlo, Melanie, Kuiper, Michael, Dahl, Hans-Henrik M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Investigative Pathology 2011
Konular:
Regular Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3157152/
https://ncbi.nlm.nih.gov/pubmed/21689626
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajpath.2011.04.002
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