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Showing 1 to 1 of 1 for “"16p11.2 microdeletion"”.
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Neurophysiological and behavioural characterisation of a 16p11.2 microdeletion rat model of autism spectrum disorder
Deletion of an approximately 600kb region of the 16p11.2 chromosome is commonly associated with autism spectrum disorder and intellectual disability. The effects of 16p11.2 microdeletion are highly variable and complex, as a result of the diversity of the 30 genes found at this locus. 16p11.2 …