📣 Try out the NEW Gateway to Research and let us know what you think.

We're looking for users to test the new service during August and September and share their feedback. Express your interest by completing this short form.

Disruption of MAGI2-RapGEF2-Rap1 signaling contributes to podocyte dysfunction in congenital nephrotic syndrome caused by mutations in MAGI2. (2019)

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