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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 2017 Jun 21; 94(6):1101-1111.e7.
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subject areas
Adolescent
Adult
Calcium-Binding Proteins
Case-Control Studies
Cell Adhesion Molecules, Neuronal
Child
Contactins
DNA Copy Number Variations
Female
Genetic Predisposition to Disease
Genome-Wide Association Study
Genotype
Humans
Male
Nerve Tissue Proteins
Neural Cell Adhesion Molecules
Odds Ratio
Tourette Syndrome
Young Adult
authors with profiles
Nancy Jean Cox