Auditory evoked-potential abnormalities in a mouse model of 22q11.2 Deletion Syndrome and their interactions with hearing impairment
Chen Lu,
Jennifer F. Linden
Abstract:BackgroundThe 22q11.2 chromosomal microdeletion is one of the strongest known genetic risk factors for schizophrenia; ∼30% of carriers develop schizophrenia in adulthood. Up to 60% of 22q11.2 deletion carriers also have mild to moderate hearing impairment, primarily from chronic middle-ear inflammation. TheDf1/+ mouse model of the 22q11.2 deletion replicates the large inter-individual variation in hearing ability observed among deletion carriers. Here we used theDf1/+mouse model of the 22q11.2 deletion to inve… Show more
Set email alert for when this publication receives citations?
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.