INF2 p.Arg214Cys mutation in a Chinese family with rapidly progressive renal failure and follow-up of renal transplantation: case report and literature review

Heterozygous mutations in the inverted formin 2 (INF2) gene are related to secondary focal segmental glomerulosclerosis (FSGS), a rare secondary disease associated with rapidly progressive renal failure.

Source: BMC Nephrology - February 4, 2021 Category: Urology & Nephrology Authors: Wenbo Zhao, Xinxin Ma, Xiaohao Zhang, Dan Luo, Jun Zhang, Ming Li, Zengchun Ye and Hui Peng Tags: Case report Source Type: research