Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications
PPFIBP1基因的双等位基因功能缺失变异会导致神经发育障碍，表现为小头畸形、癫痫和脑室周围钙化。
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2022.06.008
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; Ebrahimi Nasab, Mahya; Hussien, Haytham; Omar, Tarek E I; 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
