Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications von Rosenhahn, Erik, O'Brien, Thomas J, Zaki, Maha S, Sorge, Ina, Wieczorek, Dagmar, Rostasy, Kevin, Vitobello, Antonio, Nambot, Sophie, Alkuraya, Fowzan S, Hashem, Mais O, Alhashem, Amal, Tabarki, Brahim, Alamri, Abdullah S, Al Safar, Ayat H, Bubshait, Dalal K, Alahmady, Nada F, Gleeson, Joseph G, Abdel-Hamid, Mohamed S, Lesko, Nicole, Ygberg, Sofia, Correia, Sandrina P, Wredenberg, Anna, Alavi, Shahryar, Seyedhassani, Seyed M, Nasab, Mahya Ebrahimi, Hussien, Haytham, Omar, Tarek E, Harzallah, Ines, Touraine, Renaud, Tajsharghi, Homa, Morsy, Heba, Houlden, Henry, Shahrooei, Mohammad, Ghavideldarestani, Maryam, Abdel-Salam, Ghada M.H, Torella, Annalaura, Zanobio, Mariateresa, Terrone, Gaetano, Brunetti-Pierri, Nicola, Omrani, Abdolmajid, Hentschel, Julia, Lemke, Johannes R, Sticht, Heinrich, Abou Jamra, Rami, Brown, Andre E.X, Maroofian, Reza, Platzer, Konrad

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