Default header image

Nov 20, 2018 — Lab Research Published in PLOS One

Characterization of a novel disease-associated mutation within NPHS1 and its effects on nephrin phosphorylation and signaling has been published in PLOS One. This paper describes the molecular characterization of a newly identified mutation in the protein nephrin that causes congenital nephrotic syndrome, a disorder of the kidney. Congratulations Jim, Nikkita and Claire!