Whole-exome sequencing identifiesFOXL2,FOXA2andFOXA3as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract

Authors	Zheng Bixia, Seltzsam Steve, Wang Chunyan, Schierbaum Luca, Schneider Sophia, Wu Chen-Han Wilfred, Dai Rufeng, Connaughton Dervla M, Nakayama Makiko, Mann Nina, Stajic Natasa, Mane Shrikant, Bauer Stuart B, Tasic Velibor, Nam Hyun Joo, Shril Shirlee, Hildebrandt Friedhelm
Journal	Nephrology Dialysis Transplantation
Publication Date	2022-09-22
DOI	10.1093/ndt/gfab253