A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness

Author:

Issler Naomi,Afonso Sara,Weissman Irith,Jordan Katrin,Cebrian-Serrano Alberto,Meindl Katrin,Dahlke Eileen,Tziridis Konstantin,Yan Guanhua,Robles-López José M.,Tabernero Lydia,Patel Vaksha,Kesselheim Anne,Klootwijk Enriko D.,Stanescu Horia C.,Dumitriu Simona,Iancu Daniela,Tekman Mehmet,Mozere Monika,Jaureguiberry Graciana,Outtandy Priya,Russell Claire,Forst Anna-Lena,Sterner Christina,Heinl Elena-Sofia,Othmen Helga,Tegtmeier Ines,Reichold Markus,Schiessl Ina Maria,Limm Katharina,Oefner Peter,Witzgall Ralph,Fu Lifei,Theilig Franziska,Schilling Achim,Shuster Biton Efrat,Kalfon Limor,Fedida Ayalla,Arnon-Sheleg Elite,Ben Izhak Ofer,Magen Daniella,Anikster Yair,Schulze Holger,Ziegler Christine,Lowe Martin,Davies Benjamin,Böckenhauer Detlef,Kleta Robert,Falik Zaccai Tzipora C.,Warth Richard

Funder

Mitchell Charitable Trust

Kids Kidney Research

Kidney Research UK

Lowe Syndrome Trust

Grocers’ Charity

David and Elaine Potter Charitable Foundation

St Peter’s Trust for Kidney, Bladder, and Prostate Research

National Institute for Health Research

Deutsche Forschungsgemeinschaft

Erasmus program

Wellcome Trust

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Nephrology,General Medicine

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