Biallelic loss-of-function variants in RABGAP1cause a novel neurodevelopmental syndrome

MLA

Oh, Rachel Youjin, et al. “Biallelic Loss-of-Function Variants in RABGAP1cause a Novel Neurodevelopmental Syndrome.” Genetics in Medicine, vol. 24, no. 11, Nov. 2022, pp. 2399–407. EBSCOhost, https://doi.org/10.1016/j.gim.2022.07.024.

APA

Oh, R. Y., Deshwar, A. R., Marwaha, A., Sabha, N., Tropak, M., Hou, H., Yuki, K. E., Wilson, M. D., Rump, P., Lunsing, R., Elserafy, N., Chung, C. W. T., Hewson, S., Klein-Rodewald, T., Calzada-Wack, J., Sanz-Moreno, A., Kraiger, M., Marschall, S., Fuchs, H., … Schulze, A. (2022). Biallelic loss-of-function variants in RABGAP1cause a novel neurodevelopmental syndrome. Genetics in Medicine, 24(11), 2399–2407. https://doi.org/10.1016/j.gim.2022.07.024

Chicago

Oh, Rachel Youjin, Ashish R. Deshwar, Ashish Marwaha, Nesrin Sabha, Michael Tropak, Huayun Hou, Kyoko E. Yuki, et al. 2022. “Biallelic Loss-of-Function Variants in RABGAP1cause a Novel Neurodevelopmental Syndrome.” Genetics in Medicine 24 (11): 2399–2407. doi:10.1016/j.gim.2022.07.024.