Associated Papers
The Promise of Exome Sequencing for the Differential Diagnosis of Late-Onset End-Stage Renal Disease in Turkish Cypriots.
Kazan HH et al.
Cureus, 2025
Auxiliary genetic analysis in a Chinese adolescent NPH family by single nucleotide polymorphism screening.
Tang C et al.
Molecular Medicine Reports, 2020
The podocin V260E mutation predicts steroid resistant nephrotic syndrome in black South African children with focal segmental glomerulosclerosis.
Govender MA et al.
Communications Biology, 2019
Characterization of NPHS2 gene polymorphisms associated to steroid resistance nephrotic syndrome in Indian children.
Joshi BB et al.
Gene, 2017
Genetic effect of the NPHS2 gene variants on proteinuria in minimal change disease and immunoglobulin A nephropathy.
Zhu L et al.
Nephrology (carlton, Vic.), 2009
Clinical features and outcome of childhood minimal change nephrotic syndrome: is genetics involved?
Lahdenkari AT et al.
Pediatric Nephrology (berlin, Germany), 2005
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