Cite
A functional alternative splicing mutation in human tryptophan hydroxylase-2.
MLA
Zhang, X., et al. “A Functional Alternative Splicing Mutation in Human Tryptophan Hydroxylase-2.” Molecular Psychiatry, vol. 16, no. 12, Dec. 2011, pp. 1169–76. EBSCOhost, https://doi.org/10.1038/mp.2010.99.
APA
Zhang, X., Nicholls, P. J., Laje, G., Sotnikova, T. D., Gainetdinov, R. R., Albert, P. R., Rajkowska, G., Stockmeier, C. A., Speer, M. C., Steffens, D. C., Austin, M. C., McMahon, F. J., Krishnan, K. R. R., Garcia-Blanco, M. A., & Caron, M. G. (2011). A functional alternative splicing mutation in human tryptophan hydroxylase-2. Molecular Psychiatry, 16(12), 1169–1176. https://doi.org/10.1038/mp.2010.99
Chicago
Zhang, X, P J Nicholls, G Laje, T D Sotnikova, R R Gainetdinov, P R Albert, G Rajkowska, et al. 2011. “A Functional Alternative Splicing Mutation in Human Tryptophan Hydroxylase-2.” Molecular Psychiatry 16 (12): 1169–76. doi:10.1038/mp.2010.99.