APA (7th ed.) Citation

J, E., S, H., Y, W., A, N., M, S., M, I., . . . T, S. (2016). Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 171(6), 797. https://doi.org/10.1002/ajmg.b.32444

Chicago Style (17th ed.) Citation

J, Egawa, et al. "Rare UNC13B Variations and Risk of Schizophrenia: Whole-exome Sequencing in a Multiplex Family and Follow-up Resequencing and a Case-control Study." American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication of the International Society of Psychiatric Genetics 171, no. 6 (2016): 797. https://doi.org/10.1002/ajmg.b.32444.

MLA (9th ed.) Citation

J, Egawa, et al. "Rare UNC13B Variations and Risk of Schizophrenia: Whole-exome Sequencing in a Multiplex Family and Follow-up Resequencing and a Case-control Study." American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication of the International Society of Psychiatric Genetics, vol. 171, no. 6, 2016, p. 797, https://doi.org/10.1002/ajmg.b.32444.