Disruption of MAGI2-RapGEF2-Rap1 signaling contributes to podocyte dysfunction in congenital nephrotic syndrome caused by mutations in MAGI2. (2019)
Attributed to:
MICA: NURTuRE - changing the landscape of renal medicine to foster a unified approach to stratified medicine
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.kint.2019.03.016
PubMed Identifier: 31171376
Publication URI: http://europepmc.org/abstract/MED/31171376
Type: Journal Article/Review
Volume: 96
Parent Publication: Kidney international
Issue: 3
ISSN: 0085-2538