Neurodevelopmental disorder in an Egyptian family with a biallelic ALKBH8 variant.

MLA

Saad, Ahmed K., et al. “Neurodevelopmental Disorder in an Egyptian Family with a Biallelic ALKBH8 Variant.” American Journal of Medical Genetics. Part A, vol. 185, no. 4, Apr. 2021, pp. 1288–93. EBSCOhost, https://doi.org/10.1002/ajmg.a.62100.

APA

Saad, A. K., Marafi, D., Mitani, T., Du, H., Rafat, K., Fatih, J. M., Jhangiani, S. N., Coban-Akdemir, Z., Gibbs, R. A., Pehlivan, D., Hunter, J. V., Posey, J. E., Zaki, M. S., & Lupski, J. R. (2021). Neurodevelopmental disorder in an Egyptian family with a biallelic ALKBH8 variant. American Journal of Medical Genetics. Part A, 185(4), 1288–1293. https://doi.org/10.1002/ajmg.a.62100

Chicago

Saad, Ahmed K, Dana Marafi, Tadahiro Mitani, Haowei Du, Karima Rafat, Jawid M Fatih, Shalini N Jhangiani, et al. 2021. “Neurodevelopmental Disorder in an Egyptian Family with a Biallelic ALKBH8 Variant.” American Journal of Medical Genetics. Part A 185 (4): 1288–93. doi:10.1002/ajmg.a.62100.