rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS2 mutations account for only 15% of nephrotic syndrome cases.
|
26420286 |
2015 |
rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum.
|
24227627 |
2014 |
rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS2 gene in steroid-resistant nephrotic syndrome: prevalence, clinical course, and mutational spectrum in South-West Iranian children.
|
24072147 |
2013 |
rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome.
|
23242530 |
2013 |
rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in NPHS2 (podocin) in Mexican children with nephrotic syndrome who respond to standard steroid treatment.
|
23913389 |
2013 |
rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis.
|
23800802 |
2013 |
rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
|
22565185 |
2012 |
rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.
|
22578956 |
2012 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome.
|
23013956 |
2012 |
rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome.
|
20947785 |
2011 |
rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome.
|
20798252 |
2010 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.
|
20507940 |
2010 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome.
|
20798252 |
2010 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
R168H and V165X mutant podocin might induce different degrees of podocyte injury via different molecular mechanisms.
|
19674119 |
2009 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome.
|
19371226 |
2009 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome.
|
18216321 |
2008 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Podocin mutations in a patient with congenital nephrotic syndrome and cardiac malformation.
|
19067903 |
2008 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.
|
17899208 |
2007 |
rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.
|
17899208 |
2007 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients.
|
16810518 |
2006 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
A novel mutation of NPHS2 identified in a Chinese family.
|
15322893 |
2004 |
rs530318579
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
|
15253708 |
2004 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.
|
14978175 |
2004 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations.
|
14675423 |
2004 |
rs530318579
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
|
15253708 |
2004 |