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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
2017
176 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
16.51
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome | Researchclopedia
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University of Denver
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Medizinische Hochschule Hannover
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Medical University of Vienna
Monika Schloegelhofer
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University of Catania
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University Medical Center Groningen
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Cheston M. Berlin
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Irene A. Malaty
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