Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome by unknow
Author:unknow , Date: January 13, 2025
,Views: 4
Author:unknow
Format: pdf
Tags: Tourette Syndrome, tic disorders, neurodevelopmental disorders, genetics, structural variation, copy number variation, NRXN1, CNTN6
Publisher: Elsevier Inc.
Published: 2017-06-15T18:21:53+00:00
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