Related references
Note: Only part of the references are listed.Clinical Value of NPHS2 Analysis in Early- and Adult-Onset Steroid-Resistant Nephrotic Syndrome
Sheila Santin et al.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2011)
Familial C3 Glomerulopathy Associated with CFHR5 Mutations: Clinical Characteristics of 91 Patients in 16 Pedigrees
Yiannis Athanasiou et al.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2011)
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis
Daniel P. Gale et al.
LANCET (2010)
Clinical Features and Long-Term Outcome of Nephrotic Syndrome Associated with Heterozygous NPHS1 and NPHS2 Mutations
Gianluca Caridi et al.
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2009)
Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant
Eduardo Machuca et al.
KIDNEY INTERNATIONAL (2009)
Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis
Alkis Pierides et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION (2009)
The Association of Podocin R229Q Polymorphism With Increased Albuminuria or Reduced Estimated GFR in a Large Population-Based Sample of US Adults
Anna Koettgen et al.
AMERICAN JOURNAL OF KIDNEY DISEASES (2008)
The R229Q mutation in NPHS2 may predispose to proteinuria in thin-basement-membrane nephropathy
Stephen Tonna et al.
PEDIATRIC NEPHROLOGY (2008)
COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy
Konstantinos Voskarides et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2007)
NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis:: A HuGE review
N Franceschini et al.
GENETICS IN MEDICINE (2006)
NPHS2 R229Q functional variant is associated with microalbuminuria in the general population
AC Pereira et al.
KIDNEY INTERNATIONAL (2004)
Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus
C Bourgain et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)