Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction

Author:

Kolvenbach Caroline M.,Dworschak Gabriel C.,Frese Sandra,Japp Anna S.,Schuster Peggy,Wenzlitschke Nina,Yilmaz Öznur,Lopes Filipa M.,Pryalukhin Alexey,Schierbaum Luca,van der Zanden Loes F.M.,Kause Franziska,Schneider Ronen,Taranta-Janusz Katarzyna,Szczepańska Maria,Pawlaczyk Krzysztof,Newman William G.,Beaman Glenda M.,Stuart Helen M.,Cervellione Raimondo M.,Feitz Wouter F.J.,van Rooij Iris A.L.M.,Schreuder Michiel F.,Steffens Martijn,Weber Stefanie,Merz Waltraut M.,Feldkötter Markus,Hoppe Bernd,Thiele Holger,Altmüller Janine,Berg Christoph,Kristiansen Glen,Ludwig Michael,Reutter Heiko,Woolf Adrian S.,Hildebrandt Friedhelm,Grote Phillip,Zaniew Marcin,Odermatt Benjamin,Hilger Alina C.

Funder

Scimed

German Research Foundation

DFG

Dutch Kidney Foundation

Netherlands Organisation for Scientific Research

National Institutes of Health

DFG Excellence Cluster Cardio-Pulmonary System

Kids Kidney Research

Newlife

Horizon 2020 Marie Skłodowska-Curie Actions RENALTRACT

MRC-Wellcome Trust Human Developmental Biology Resource

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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