Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract.
Marcin KołbucMateusz F KołekRafał MotykaBeata BieniaśSandra HabbigKathrin BurgmaierLarisa PrikhodinaSvetlana PapizhVelibor TasicChristine OkornMaria SzczepańskaKatarzyna Kiliś-PstrusińskaAnna WasilewskaPiotr AdamczykMarcin TkaczykMałgorzata Pańczyk-TomaszewskaMonika MiklaszewskaKrzysztof PawlaczykEwelina Bukowska-OlechAleksander JamsheerAugustina JankauskieneJens KönigHae Il CheongYo Han AhnSophie KasparPrzemysław SikoraBodo B BeckMarcin ZaniewPublished in: Pediatric nephrology (Berlin, Germany) (2024)
This study developed a simple tool for predicting HNF1B mutations in children and young adults with CAKUT.
Keyphrases