Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome - Concepedia

Concepedia

Publication | Open Access

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

DOI Full Paper Access

176

Citations

48

References

2017

Year

Alden Y. Huang, Dongmei Yu, Lea K. Davis, Jae Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason Chen,

Genetic DisorderCntn6 Increase RiskGeneticsGenetic EpidemiologyPsychiatric GeneticsNeurologyNeuroscienceMedicineTourette SyndromeTic Disorder

References

	Year	Citations

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