Phenotypic expansion in DDX3X – a common cause of intellectual disability in females

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Funding Information Research reported in this manuscript was supported by the NIH Common Fund, through the Office of Strategic Coordination/Office of the NIH Director under Award Number U01HG007709, and the National Human Genome Research Institute (NHGRI)/National Heart Lung and Blood Institute (NHLBI) UM1 HG006542 to the Baylor Hopkins Center for Mendelian Genomics. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. J. E. P. was supported by K08 HG008986 through the National Human Genome Research Institute.