|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
CLINVAR |
NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome.
|
23242530 |
2013 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
CausalMutation
|
disease |
CLINVAR |
NPHS2 gene in steroid-resistant nephrotic syndrome: prevalence, clinical course, and mutational spectrum in South-West Iranian children.
|
24072147 |
2013 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
CausalMutation
|
disease |
CLINVAR |
Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population.
|
23645318 |
2013 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
UNIPROT |
NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis.
|
23800802 |
2013 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
CLINVAR |
NPHS2 gene in steroid-resistant nephrotic syndrome: prevalence, clinical course, and mutational spectrum in South-West Iranian children.
|
24072147 |
2013 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
CausalMutation
|
disease |
CLINVAR |
A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families.
|
23595123 |
2013 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
CLINVAR |
Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population.
|
23645318 |
2013 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
CausalMutation
|
disease |
CLINVAR |
NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome.
|
23242530 |
2013 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
CausalMutation
|
disease |
CLINVAR |
Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
|
23515051 |
2013 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
CLINVAR |
Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
|
23515051 |
2013 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
CausalMutation
|
disease |
CLINVAR |
Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.
|
22578956 |
2012 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
CLINVAR |
NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome.
|
23013956 |
2012 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
UNIPROT |
Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.
|
22578956 |
2012 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
BEFREE |
Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.
|
22578956 |
2012 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
UNIPROT |
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
|
22565185 |
2012 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
CausalMutation
|
disease |
CLINVAR |
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
|
22565185 |
2012 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
CLINVAR |
Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.
|
22578956 |
2012 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
CLINVAR |
Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
|
21415313 |
2011 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
CLINVAR |
Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.
|
21355056 |
2011 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
CLINVAR |
Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome.
|
20947785 |
2011 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
CLINVAR |
Anemia in congenital nephrotic syndrome: role of urinary copper and ceruloplasmin loss.
|
21636722 |
2011 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
CausalMutation
|
disease |
CLINVAR |
Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome.
|
20947785 |
2011 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
UNIPROT |
Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome.
|
20947785 |
2011 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
GeneticVariation
|
disease |
CLINVAR |
Plasmapheresis-induced clinical improvement in a patient with steroid-resistant nephrotic syndrome due to podocin (NPHS2) gene mutation.
|
21171529 |
2010 |
|
| Entrez Id: |
7827 |
| Gene Symbol: |
NPHS2 |
NPHS2
|
0.680 |
CausalMutation
|
disease |
CLINVAR |
Plasmapheresis-induced clinical improvement in a patient with steroid-resistant nephrotic syndrome due to podocin (NPHS2) gene mutation.
|
21171529 |
2010 |