Sh3pxd2b Mice Are a Model for Craniofacial Dysmorphology and Otitis Media

Craniofacial defects that occur through gene mutation during development increase vulnerability to eustachian tube dysfunction. These defects can lead to an increased incidence of otitis media. We examined the effects of a mutation in the Sh3pxd2b gene (Sh3pxd2b(nee)) on the progression of otitis me...

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Detalles Bibliográficos
Autores principales: Yang, Bin, Tian, Cong, Zhang, Zhi-guang, Han, Feng-chan, Azem, Rami, Yu, Heping, Zheng, Ye, Jin, Ge, Arnold, James E., Zheng, Qing Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144925/
https://www.ncbi.nlm.nih.gov/pubmed/21818352
http://dx.doi.org/10.1371/journal.pone.0022622

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