Cite
De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy
MLA
Victor Murcia Pienkowski, et al. “De Novo and Bi-Allelic Variants in AP1G1 Cause Neurodevelopmental Disorder with Developmental Delay, Intellectual Disability, and Epilepsy.” American Journal of Human Genetics, vol. 108, no. 7, July 2021, pp. 1330–41. EBSCOhost, https://doi.org/10.1016/j.ajhg.2021.05.007.
APA
Victor Murcia Pienkowski, Saima Riazuddin, Matthew J. Schultz, S. Amer Riazuddin, Foong-Yen Lim, Nicola Perrotti, Claudia Gonzaga-Jauregui, Muhammad A. Usmani, Zubair M. Ahmed, Hane Lee, Erik G. Puffenberger, Anneke J.A. Kievit, Tommaso Pippucci, Pamela Magini, Emma Colao, M. Mahdi Motazacker, Rebecca Hernan, Mureed Hussain, Karlla W. Brigatti, … Sheikh Riazuddin. (2021). De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy. American Journal of Human Genetics, 108(7), 1330–1341. https://doi.org/10.1016/j.ajhg.2021.05.007
Chicago
Victor Murcia Pienkowski, Saima Riazuddin, Matthew J. Schultz, S. Amer Riazuddin, Foong-Yen Lim, Nicola Perrotti, Claudia Gonzaga-Jauregui, et al. 2021. “De Novo and Bi-Allelic Variants in AP1G1 Cause Neurodevelopmental Disorder with Developmental Delay, Intellectual Disability, and Epilepsy.” American Journal of Human Genetics 108 (7): 1330–41. doi:10.1016/j.ajhg.2021.05.007.