<scp>El‐Hattab‐Alkuraya</scp> syndrome caused by biallelic <scp><i>WDR45B</i></scp> pathogenic variants: Further delineation of the phenotype and genotype
Mohammed Almannai(King Fahd Medical City), Ayman W. El‐Hattab(Khalifa University of Science and Technology), Jennifer E. Posey(Baylor College of Medicine), Kolsoum Saeidi(Kerman University of Medical Sciences), Joseph G. Gleeson(Howard Hughes Medical Institute), Maha S. Zaki(National Research Centre), Wendy K. Chung(Columbia University), Dana Marafi(Baylor College of Medicine), Asma Al Madhi(King Fahd Medical City), Daniel G. Calame, Ghada M. H. Abdel‐Salam(National Research Centre), Haluk Kavuş(Columbia University Irving Medical Center), Ruizhi Duan(Baylor College of Medicine), Isabella Herman(Texas Children's Hospital), Hasnaa M. Elbendary(National Human Genome Research Institute), Ali Al‐Otaibi(King Fahd Medical City), Ibrahim Hegazy(Agricultural Genetic Engineering Research Institute), Henry Houlden(University College London), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Jill V. Hunter(Baylor College of Medicine), Felix Levesque(Royal University Hospital), Hager M. Abou Al‐Seood(King Fahd Medical City), James R. Lupski(Baylor College of Medicine), Ali Alasmari(King Fahd Medical City), Aqeela AlHashim(King Fahd Medical City)
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