Cite
De novo, heterozygous, loss-of-function mutations in SYNGAP1 cause a syndromic form of intellectual disability.
MLA
Parker, Michael J., et al. “De Novo, Heterozygous, Loss-of-Function Mutations in SYNGAP1 Cause a Syndromic Form of Intellectual Disability.” American Journal of Medical Genetics. Part A, vol. 167A, no. 10, Oct. 2015, pp. 2231–37. EBSCOhost, https://doi.org/10.1002/ajmg.a.37189.
APA
Parker, M. J., Fryer, A. E., Shears, D. J., Lachlan, K. L., McKee, S. A., Magee, A. C., Mohammed, S., Vasudevan, P. C., Park, S.-M., Benoit, V., Lederer, D., Maystadt, I., Study, D., & FitzPatrick, D. R. (2015). De novo, heterozygous, loss-of-function mutations in SYNGAP1 cause a syndromic form of intellectual disability. American Journal of Medical Genetics. Part A, 167A(10), 2231–2237. https://doi.org/10.1002/ajmg.a.37189
Chicago
Parker, Michael J, Alan E Fryer, Deborah J Shears, Katherine L Lachlan, Shane A McKee, Alex C Magee, Shehla Mohammed, et al. 2015. “De Novo, Heterozygous, Loss-of-Function Mutations in SYNGAP1 Cause a Syndromic Form of Intellectual Disability.” American Journal of Medical Genetics. Part A 167A (10): 2231–37. doi:10.1002/ajmg.a.37189.