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Article

NPHS2 Mutations: A Closer Look to Latin American Countries.

BioMed research international - 1 Jan 2017

Guaragna Mara Sanches, Lutaif Anna Cristina G B, Maciel-Guerra Andréa T, Belangero Vera M S, Guerra-Júnior Gil, De Mello Maricilda P

Abstract excerpt

Nephrotic syndrome is one of the most common kidney pathologies in childhood, being characterized by proteinuria, edema, and hypoalbuminemia. In clinical practice, it is divided into two categories based on the response to steroid therapy: steroid-sensitive and steroid resistant. Inherited impairments of proteins located in the glomerular filtration barrier have been identified as important causes of nephrotic...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 28785586
DOI: 10.1155/2017/7518789
PMCID: PMC5529630

Genes

NPHS2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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