Skip to content
VuFind
    • English
    • Deutsch
    • Español
    • Français
    • Italiano
    • 日本語
    • Nederlands
    • Português
    • Português (Brasil)
    • 中文(简体)
    • 中文(繁體)
    • Türkçe
    • עברית
    • Gaeilge
    • Cymraeg
    • Ελληνικά
    • Català
    • Euskara
    • Русский
    • Čeština
    • Suomi
    • Svenska
    • polski
    • Dansk
    • slovenščina
    • اللغة العربية
    • বাংলা
    • Galego
    • Tiếng Việt
    • Hrvatski
    • हिंदी
    • Հայերէն
    • Українська
    • Sámegiella
    • Монгол
Advanced
  • Human C-terminal CUBN varian...
  • Cite this
  • Text this
  • Email this
  • Print
  • Export Record
    • Export to RefWorks
    • Export to EndNoteWeb
    • Export to EndNote
  • Permanent link
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

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

Bibliographic Details
Main Authors: Mathilda Bedin, Olivia Boyer, Aude Servais, Yong Li, Laure Villoing-Gaudé, Marie-Josephe Tête, Alexandra Cambier, Julien Hogan, Veronique Baudouin, Saoussen Krid, Albert Bensman, Florie Lammens, Ferielle Louillet, Bruno Ranchin, Cecile Vigneau, Iseline Bouteau, Corinne Isnard-Bagnis, Christoph J. Mache, Tobias Schäfer, Lars Pape, Markus Gödel, Tobias B. Huber, Marcus Benz, Günter Klaus, Matthias Hansen, Kay Latta, Olivier Gribouval, Vincent Morinière, Carole Tournant, Maik Grohmann, Elisa Kuhn, Timo Wagner, Christine Bole-Feysot, Fabienne Jabot-Hanin, Patrick Nitschké, Tarunveer S. Ahluwalia, Anna Köttgen, Christian Brix Folsted Andersen, Carsten Bergmann, Corinne Antignac, Matias Simons
Format: Article
Language:English
Published: American Society for Clinical Investigation 2022-06-01
Series:The Journal of Clinical Investigation
Online Access:https://doi.org/10.1172/JCI161852
  • Holdings
  • Description
  • Similar Items
  • Staff View

Internet

https://doi.org/10.1172/JCI161852

Similar Items

  • CUBN mutation, a genetic cause of persistent proteinuria in children
    by: Jin-Soon Suh
    Published: (2024-10-01)
  • Identification of novel pathogenic variants of CUBN in patients with isolated proteinuria
    by: Huihui Yang, et al.
    Published: (2024-03-01)
  • Isolated benign persistent proteinuria with novel association of CUBN (cubilin) variants
    by: Vivian Shi, et al.
    Published: (2023-06-01)
  • Isolated proteinuria due to CUBN homozygous mutation – challenging the investigative paradigm
    by: Kushani Jayasinghe, et al.
    Published: (2019-08-01)
  • Novel pathogenic variants in CUBN uncouple proteinuria from renal function
    by: Chun Gan, et al.
    Published: (2022-10-01)

Search Options

  • Search History
  • Advanced Search

Find More

  • Browse the Catalog
  • Browse Alphabetically
  • Explore Channels
  • Course Reserves
  • New Items

Need Help?

  • Search Tips
  • Ask a Librarian
  • FAQs