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Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

Journal: Journal of Clinical Investigation

Published: 2019-10-15

DOI: 10.1172/jci129937

Affiliations: 28

Authors: 41

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Institutions Share
Laboratory of Molecular Bases of Hereditary Kidney Diseases, Imagine Institute, France 0.09
Laboratory of Epithelial Biology and Disease, Imagine Institute, France 0.07
Robert Debré University Hospital, France 0.07
Hopital Necker, France 0.07
Bioscientia Center for Human Genetics, Germany 0.07
Hôpital Necker-Enfants Malades, France 0.06
Institute of Genetic Epidemiology, Uni Freiburg, Germany 0.05
Department of Internal Medicine, UHH, Germany 0.05
Structure Fédérative de Recherche Necker (SFR Necker), France 0.04
Bioinformatics Platform, Imagine Institute, France 0.04
Klinik für Kinder- und Jugendmedizin I Marburg, UKGM, Germany 0.02
Department of Biomedicine, AU, Denmark 0.02
Steno Diabetes Center A/S, Denmark 0.02
Clementine-Kinderhospital, Germany 0.02
KfH-Nierenzentrum für Kinder und Jugendliche Frankfurt, Germany 0.02
Clinic for Pediatric Kidney, Liver and Metabolic Diseases and Neuropediatrics, MHH, Germany 0.02
Kindernephrologie in Dachau - Dr. med. Marcus Benz, Germany 0.02
University Medical Center Freiburg, Germany 0.02
Department of Pediatrics and Adolescent Medicine, Med Uni Graz, Austria 0.02
AP-HP Pitié-Salpêtrière Hospital - Charles-Foix, France 0.02
CHU de Poitiers, France 0.02
Institut de Recherche en Santé, Environnement et Travail (IRSET), France 0.02
Lyon University Hospital (HCL), France 0.02
Rouen University Hospital-Charles Nicolle (CHU de Rouen), France 0.02
Centre Hospitalier Régional Universitaire de Lille (CHRU de Lille), France 0.02
Fachbereich Humangenetische Diagnostik, Limbach Gruppe SE, Germany 0.02
Internal Medicine, Uni Freiburg, Germany 0.01

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