M. Gou

A case report of CRB2 mutation identified in a Chinese boy with focal segmental glomerulosclerosis

J. Fan, Rong Fu, F. Ren, 2018, Medicine.

Novel NPHS1 splice site mutations in a Chinese child with congenital nephrotic syndrome.

R. Fu, J. Liu, Y. Luan, 2015, Genetics and molecular research : GMR.

Novel NPHS 1 splice site mutations in a Chinese child with congenital nephrotic syndrome

R. Fu, Y. Luan, J. Liu, 2015 .

Mutation of NPHS1 gene in a Chinese child with congenital nephrotic syndrome

Hui Guo, Jixiang Xu, R. Fu, 2015 .