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A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness

  • Naomi Issler
  • , Sara Afonso
  • , Irith Weissman
  • , Katrin Jordan
  • , Alberto Cebrian-Serrano
  • , Katrin Meindl
  • , Eileen Dahlke
  • , Konstantin Tziridis
  • , Guanhua Yan
  • , Jose M. Robles-Lopez
  • , Lydia Tabernero
  • , Vaksha Patel
  • , Anne Kesselheim
  • , Enriko D. Klootwijk
  • , Horia C. Stanescu
  • , Simona Dumitriu
  • , Daniela Iancu
  • , Mehmet Tekman
  • , Monika Mozere
  • , Graciana Jaureguiberry
    • Priya Outtandy, Claire Russell, Anna Lena Forst, Christina Sterner, Elena Sofia Heinl, Helga Othmen, Ines Tegtmeier, Markus Reichold, Ina Maria Schiessl, Katharina Limm, Peter Oefner, Ralph Witzgall, Lifei Fu, Franziska Theilig, Achim Schilling, Efrat Shuster Biton, Limor Kalfon, Ayalla Fedida, Elite Arnon-Sheleg, Ofer Ben Izhak, Daniella Magen, Yair Anikster, Holger Schulze, Christine Ziegler, Martin Lowe, Benjamin Davies, Detlef Bockenhauer, Robert Kleta*, Tzipora C. Falik Zaccai, Richard Warth*
*Corresponding author for this work
  • University College London
  • University of Regensburg
  • Galilee Medical Center
  • University of Oxford
  • Kiel University
  • Friedrich-Alexander University Erlangen-Nürnberg
  • University of Manchester
  • Royal Veterinary College University of London
  • Western Galilee Medical Center of Nahariya
  • Rambam Health Care Campus Israel
  • Sheba Medical Center at Tel Hashomer
  • Bar-Ilan University

Research output: Contribution to journal › Article › peer-review

12 Scopus citations

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology