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Chronic renal failure of unknown origin is caused by HNF1B mutations in 9% of adult patients: A single centre cohort analysis |
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| Authors: | Claudio Musetti Marco Quaglia Simona Mellone Alessia Pagani Ileana Fusco Alice Monzani Mara Giordano Piero Stratta |
| Affiliation: | 1. Department of Translational Medicine, Nephrology and Transplantation, Hospital ‘Maggiore della Carità’, , Novara, NO, Italy;2. Laboratory of Genetics, Department of Health Sciences and IRCAD, University of Eastern Piedmont ‘Amedeo Avogadro’, , Novara, NO, Italy;3. Division of Pediatrics, Department of Health Sciences, University of ‘Piemonte Orientale Amedeo Avogadro’, , Novara, NO, Italy |
| Abstract: | |
| Keywords: | chronic kidney disease end‐stage renal disease (ESRD) hepatocyte nuclear factor‐1β gene (HNF1B) hereditary cystic diseases renal malformations |