Associated Papers
NPHS2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum.
Bouchireb K et al.
Human Mutation, 2014
Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
Chernin G et al.
Pediatric Nephrology (berlin, Germany), 2008
NPHS2 variation in sporadic focal segmental glomerulosclerosis.
McKenzie LM et al.
Journal of the American Society of Nephrology : Jasn, 2007
Lack of association between NPHS2 gene polymorphisms and Henoch-Schönlein purpura nephritis.
Zhang Y et al.
Archives of Dermatological Research, 2007
NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review.
Franceschini N et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2006
Identification of podocin (NPHS2) gene mutations in African Americans with nondiabetic end-stage renal disease.
Dusel JA et al.
Kidney International, 2005
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