Associated Papers
NPHS2 variation in Chinese southern infants with late steroid-resistant nephrotic syndrome.
Dai Y et al.
Renal Failure, 2014
Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis.
Caminsky N et al.
F1000research, 2014
25717368 (PubMed )
Supplement: f1000research-3-6038-s0000.tgz › e0d3facd-5877-477e-9217-8c5aa68746f2_Supplementary-Tables-11112014.zip › Supplementary-Tables-and-Figures-11112014 › Supplementary_Table_3._Indels__Duplications_and_Multinucleotide_VariantsV2.xlsx › Supplementary_Table_3
Clinical course and NPHS2 analysis in patients with late steroid-resistant nephrotic syndrome.
Schwaderer P et al.
Pediatric Nephrology (berlin, Germany), 2008
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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