HNF1B nephropathy: for which congenital renal anomalies is genetic analysis advisable?

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Title: HNF1B nephropathy: for which congenital renal anomalies is genetic analysis advisable?
Authors: Flögelova H; Department of Pediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Zdravotniku 248/7, 77900, Olomouc, Czech Republic. Hana.Flogelova@seznam.cz., Strasil R; Department of Pediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Zdravotniku 248/7, 77900, Olomouc, Czech Republic.; Institute of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Zdravotniku 248/7, 77900, Olomouc, Czech Republic.
Source: Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2026 Feb; Vol. 41 (2), pp. 263-265. Date of Electronic Publication: 2025 Jul 29.
Publication Type: Editorial
Journal Info: Publisher: Springer International Country of Publication: Germany NLM ID: 8708728 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-198X (Electronic) Linking ISSN: 0931041X NLM ISO Abbreviation: Pediatr Nephrol Subsets: MEDLINE; In Process
Database: MEDLINE Ultimate
Description
ISSN:1432-198X
DOI:10.1007/s00467-025-06915-x