RSRC1 loss-of-function variants cause mild to moderate autosomal recessive intellectual disability
Marcello Scala(Hospital for Sick Children), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Anne M. Comi(Kennedy Krieger Institute), Katie B. Williams(UW Health University Hospital), Karlla W. Brigatti(Clinic for Special Children), Maha S. Zaki(National Research Centre), Marta Biderman Waberski(National Institutes of Health), Dana Marafi(Baylor College of Medicine), Fan Xia(Baylor College of Medicine), Heba Hosny(The National Institute of Neuromotor System), Queen Square Genomics(National Hospital for Neurology and Neurosurgery), Atiye Eslahi(Mashhad University of Medical Sciences), Hasnaa M. Elbendary(National Human Genome Research Institute), Jill A. Rosenfeld(Baylor College of Medicine), Sheikh Riazuddin(University of the Punjab), Mohsin Shahzad(University of the Punjab), Zineb Ammous, Majid Mojarrad(Mashhad University of Medical Sciences), Julie S. Cohen(Kennedy Krieger Institute), Muhammad A. Usmani(University of Maryland, Baltimore), Henry Houlden(University College London), Saima Riazuddin(University of Maryland, Baltimore), Joseph G. Gleeson(Howard Hughes Medical Institute), Vincenzo Salpietro(University College London), Richard Person(Baylor College of Medicine), Laura Poskitt(Clinic for Special Children), Valentina Stanley(Children’s Institute), Erik G. Puffenberger(Clinic for Special Children)
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