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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
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 |