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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

Alden Y Huang1, Dongmei Yu2, Lea K Davis3

  • 1Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, CA 90095, USA; Bioinformatics Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA 90095, USA.

Neuron
|June 23, 2017
PubMed

Keywords:
CNTN6NRXN1Tourette Syndromecopy number variationgeneticsneurodevelopmental disordersstructural variationtic disorders

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