Items where Author is "Outtandy, Priya"

Article

Issler, Naomi and Afonso, Sara and Weissman, Irith and Jordan, Katrin and Cebrian-Serrano, Alberto and Meindl, Katrin and Dahlke, Eileen and Tziridis, Konstantin and Yan, Guanhua and Robles-Lopez, Jose M. and Tabernero, Lydia and Patel, Vaksha and Kesselheim, Anne and Klootwijk, Enriko D. and Stanescu, Horia C. and Dumitriu, Simona and Iancu, Daniela and Tekman, Mehmet and Mozere, Monika and Jaureguiberry, Graciana and Outtandy, Priya and Russell, Claire and Forst, Anna-Lena and Sterner, Christina and Heinl, Elena-Sofia and Othmen, Helga and Tegtmeier, Ines and Reichold, Markus and Schiessl, Ina Maria and Limm, Katharina and Oefner, Peter and Witzgall, Ralph and Fu, Lifei and Theilig, Franziska and Schilling, Achim and Biton, Efrat Shuster and Kalfon, Limor and Fedida, Ayalla and Arnon-Sheleg, Elite and Ben Izhak, Ofer and Magen, Daniella and Anikster, Yair and Schulze, Holger and Ziegler, Christine and Lowe, Martin and Davies, Benjamin and Boeckenhauer, Detlef and Kleta, Robert and Zaccai, Tzipora C. Falik and Warth, Richard (2022) A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 33 (4). pp. 732-745. ISSN 1046-6673, 1533-3450