Article

Development of a tool for predicting HNF1B mutations in children with congenital anomalies of the kidneys and urinary tract – a retrospective multicenter study

2023-09-14

Abstract excerpt

<title>Abstract</title> <p><bold>Background </bold>The diagnosis of <italic>HNF1B</italic> disease is a challenge. We aimed to developa tool for predicting <italic>HNF1B</italic> mutations in children with congenital abnormalities of the kidneys and urinary tract (CAKUT). <bold>Methods</bold><italic> </italic>The clinical and laboratory data from 234 children and young adults with known <italic>HNF1B</italic> mut...

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Literature Corpus work: 18350616-3fc8-5639-88f0-e0b1fdcedfaa
DOI: 10.21203/rs.3.rs-3344410/v1

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