GeneticsbioRxiv
Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome
Alden Y Huang, Dongmei Yu, Lea K Davis…·Danielle C Cath
The paper identifies two rare copy number variants, NRXN1 and CNTN6, significantly increasing the risk of Tourette syndrome in a European ancestry sample.
DOI 10.1016/j.neuron.2017.06.010