Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome

Yang, N; Wu, N; Dong, SS; Zhang, L; Zhao, YX; Chen, WS; Du, RQ; Song, CC; Ren, XJ; Liu, JQ; Pehlivan, D; Liu, ZL; Rao, J; Wang, CY; Zhao, S; Breman, AM; Xue, HD; Sun, H; Shen, JX; Zhang, SY; Posey, JE; Xu, H; Jin, L; Zhang, JG; Liu, PF; Sanna-Cherchi, S; Qiu, GX; Wu, ZH; Lupski, JR; Zhang, F

Zhang, F (corresponding author), Fudan Univ, Obstet & Gynecol Hosp, Shanghai 200011, Peoples R China.

KIDNEY INTERNATIONAL, 2020; 98 (4): 1020

Abstract

Congenital anomalies of the kidney and urinary tract (CAKUTs) are the most common cause of chronic kidney disease in children. Human 16p11.2 deletions......

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