Cite
Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes.
MLA
Moya, Pablo R., et al. “Rare Missense Neuronal Cadherin Gene (CDH2) Variants in Specific Obsessive-Compulsive Disorder and Tourette Disorder Phenotypes.” European Journal of Human Genetics, vol. 21, no. 8, Aug. 2013, pp. 850–54. EBSCOhost, https://doi.org/10.1038/ejhg.2012.245.
APA
Moya, P. R., Dodman, N. H., Timpano, K. R., Rubenstein, L. M., Rana, Z., Fried, R. L., Reichardt, L. F., Heiman, G. A., Tischfield, J. A., King, R. A., Galdzicka, M., Ginns, E. I., & Wendland, J. R. (2013). Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes. European Journal of Human Genetics, 21(8), 850–854. https://doi.org/10.1038/ejhg.2012.245
Chicago
Moya, Pablo R, Nicholas H Dodman, Kiara R Timpano, Liza M Rubenstein, Zaker Rana, Ruby L Fried, Louis F Reichardt, et al. 2013. “Rare Missense Neuronal Cadherin Gene (CDH2) Variants in Specific Obsessive-Compulsive Disorder and Tourette Disorder Phenotypes.” European Journal of Human Genetics 21 (8): 850–54. doi:10.1038/ejhg.2012.245.