Hearing Loss in a Mouse Model of 22q11.2 Deletion Syndrome

22q11.2 Deletion Syndrome (22q11DS) arises from an interstitial chromosomal microdeletion encompassing at least 30 genes. This disorder is one of the most significant known cytogenetic risk factors for schizophrenia, and can also cause heart abnormalities, cognitive deficits, hearing difficulties, a...

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Detalles Bibliográficos
Autores principales: Fuchs, Jennifer C., Zinnamon, Fhatarah A., Taylor, Ruth R., Ivins, Sarah, Scambler, Peter J., Forge, Andrew, Tucker, Abigail S., Linden, Jennifer F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3828191/
https://www.ncbi.nlm.nih.gov/pubmed/24244619
http://dx.doi.org/10.1371/journal.pone.0080104

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3828191/
https://www.ncbi.nlm.nih.gov/pubmed/24244619
http://dx.doi.org/10.1371/journal.pone.0080104

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