Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association

Pawaree Saisawat(University of Michigan), Friedhelm Hildebrandt(Boston Children's Hospital), S. Natarajan(University of Michigan), Tracie Pennimpede, Erwin Brosens(Erasmus MC), Gabriel C. Dworschak(University of Bonn), Iris A.L.M. van Rooij(Radboud University Nijmegen), Eberhard Schmiedeke(Klinikum Bremen-Mitte), Hugo A. Heij(Emma Kinderziekenhuis), Stefan Holland‐Cunz(Heidelberg University), Alina C. Hilger(Universitätsklinikum Erlangen), Dick Tibboel(Erasmus University Rotterdam), Enrika Bartels(University of Bonn), Dominik Schmidt(University of Bonn), Carlo Marcelis(Radboud University Nijmegen), Sabine Grasshoff‐Derr(Universitätsklinikum Würzburg), Michael Ludwig(University of Chicago), Stefanie Märzheuser(Charité - Universitätsmedizin Berlin), Stefan Kohl(Boston Children's Hospital), Radovan Bogdanović(Institute of Public Health of Serbia), Nataša Stajić, Danilo Swann Matassa(Federico II University Hospital), Heon Yung Gee(Yonsei University), Ethan D. Sperry(University of Michigan), Daw‐Yang Hwang(Kaohsiung Medical University Chung-Ho Memorial Hospital), Ivo de Blaauw(Radboud University Nijmegen), Annelies de Klein(Erasmus MC), Heiko Reutter(University Hospital Bonn), Velibor Tasić(University Clinic of Traumatology), Bernhard G. Herrmann(Max Planck Institute for Molecular Genetics), Benjamin D. Solomon(National Human Genome Research Institute), Markus M. Nöthen(University of Bonn), Markus Draaken(University of Bonn), Charlotte H. W. Wijers(Radboud University Nijmegen), Franca Esposito(Federico II University Hospital)
Kidney International
October 23, 2013
Cited by 128


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