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Article

CG/CA genotypes represent novel markers in the NPHS2 gene region associated with nephrotic syndrome.

Journal of genetics - 1 Jan 2020

Chamgordani Leila Esmaeli, Ebrahimi Nasim, Amirmahani Farzane, Vallian Sadeq

Abstract excerpt

Nephrotic syndrome (NS) is considered as a primary disease of the kidney that represents a heterogeneous group of glomerular disorders occurring mainly in children. It is generally divided into steroid-sensitive and steroid-resistant forms, depending upon the patient's response to steroid therapy. Among the genes involved, the NPHS2 gene has been reported as the causative gene in steroid resistant form of...

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Identifiers

PMID: 32482922

Genes

NPHS2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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