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Koziell, A., Grech, V., Hussain, S., Lee, G., Lenkkeri, U., Tryggvason, K., et al. (2002) Genotype/Phenotype Correlations of NPHS1 and NPHS2 Mutations in Nephrotic Syndrome Advocate a Functional Inter-Relationship in Glomerular Filtration. Human Molecular Genetics, 11, 379-388.
http://dx.doi.org/10.1093/hmg/11.4.379

has been cited by the following article:

• TITLE: Congenital Nephrotic Syndrome of the Finnish Type: A Greek Case Report

  AUTHORS: Sofia Melina Stasinou, George Valasoulis, Ioannis Georgiou, Kyrgiou Maria, Evangelos Paraskevaidis, Nikolaos Plachouras

  KEYWORDS: NPHS1 Gene, Congenital Nephrotic Syndrome, Kidney Ultrasound Findings

  JOURNAL NAME: Health, Vol.6 No.12, June 23, 2014

  ABSTRACT: Congenital Nephrotic Syndrome Type 1 (Congenital Nephrotic Syndrome of the Finnish Type—CNF) is an autosomal recessive disorder encoding by nephrin gene mutation which is a (transmembrane protein 1-homolog—NPHS1) structural component of the slit diaphragm responsible for the proper functioning of the renal filtration barrier. In NPHS1 kidneys there is an effacement of the foot processes of the podocytes and impaired glomerular filtration barrier leading to antenatal manifestations and end-renal stage of disease after birth. We present a case of this disease where sonographic appearance of the fetal kidneys had alerted the experts for further genetic investigation for congenital nephrotic syndrome.