Associated Papers
Disruption of MAGI2-RapGEF2-Rap1 signaling contributes to podocyte dysfunction in congenital nephrotic syndrome caused by mutations in MAGI2.
Zhu B et al.
Kidney International, 2019
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment.
Ashraf S et al.
Nature Communications, 2018
Select a paper to view details