Hearing loss in a mouse model of 22q11.2 Deletion Syndrome.

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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Bibliographic Details
Main Authors: Jennifer C Fuchs, Fhatarah A Zinnamon, Ruth R Taylor, Sarah Ivins, Peter J Scambler, Andrew Forge, Abigail S Tucker, Jennifer F Linden
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3828191?pdf=render

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http://europepmc.org/articles/PMC3828191?pdf=render

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