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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Detalhes bibliográficos
Main Authors: Manji, Shehnaaz S.M., Miller, Kerry A., Williams, Louise H., Andreasen, Lotte, Siboe, Maria, Rose, Elizabeth, Bahlo, Melanie, Kuiper, Michael, Dahl, Hans-Henrik M.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2011
Assuntos:
Regular Article
Acesso em linha: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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