De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy
Titel:
De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy
Auteur:
Usmani, Muhammad A. Ahmed, Zubair M. Magini, Pamela Pienkowski, Victor Murcia Rasmussen, Kristen J. Hernan, Rebecca Rasheed, Faiza Hussain, Mureed Shahzad, Mohsin Lanpher, Brendan C. Niu, Zhiyv Lim, Foong-Yen Pippucci, Tommaso Ploski, Rafal Kraus, Verena Matuszewska, Karolina Palombo, Flavia Kianmahd, Jessica Martinez-Agosto, Julian A. Lee, Hane Colao, Emma Motazacker, M. Mahdi Brigatti, Karlla W. Puffenberger, Erik G. Riazuddin, S. Amer Gonzaga-Jauregui, Claudia Chung, Wendy K. Wagner, Matias Schultz, Matthew J. Seri, Marco Kievit, Anneke J.A. Perrotti, Nicola Klein Wassink-Ruiter, J.S. van Bokhoven, Hans Riazuddin, Sheikh Riazuddin, Saima