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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書誌詳細
主要な著者: Manji, Shehnaaz S.M., Miller, Kerry A., Williams, Louise H., Andreasen, Lotte, Siboe, Maria, Rose, Elizabeth, Bahlo, Melanie, Kuiper, Michael, Dahl, Hans-Henrik M.
フォーマット: Artigo
言語:Inglês
出版事項: American Society for Investigative Pathology 2011
主題:
Regular Article
オンライン･アクセス: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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