Article

Implication of<i>FOXD2</i>dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

2023-03-22

Abstract excerpt

<h4>Background</h4> Congenital anomalies of the kidney and urinary tract (CAKUT) are the predominant cause for chronic kidney disease below 30 years of age. Many monogenic forms have been discovered mainly due to comprehensive genetic testing like exome sequencing (ES). However, disease-causing variants in known disease-associated genes still only explain a proportion of cases. Aim of this study was to unravel the...

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Literature Corpus work: 828a508c-f1ac-58b2-bcb6-4797083e057f
DOI: 10.1101/2023.03.21.23287206

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