Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)
Chen‐Han Wilfred Wu(Boston Children's Hospital), Friedhelm Hildebrandt(Boston Children's Hospital), Verena Klämbt(Boston Children's Hospital), Jameela A. Kari(King Abdulaziz University), Prabha Senguttuva, Rufeng Dai(Boston Children's Hospital), Stuart B. Bauer(Boston Children's Hospital), Ethan Lai(Boston Children's Hospital), Steve Seltzsam(Boston Children's Hospital), Sherif El Desoky(King Abdulaziz University), Dervla M. Connaughton(Western University), Franziska Kause(Boston Children's Hospital), Shirlee Shril(MACOM (United States)), Deborah R. Stein, Aravind Selvin(Tamil Nadu Dr. M.G.R. Medical University), Caroline M. Kolvenbach(Boston Children's Hospital), Velibor Tasić(University Clinic of Traumatology), Olaf A. Bodamer(Broad Institute), Chunyan Wang(Washington University in St. Louis), Nina Mann(Boston Children's Hospital), Makiko Nakayama, Isabel Ottlewski(Boston Children's Hospital)
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