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Article

Association of a Haplotype in the NR3C2 Gene, Encoding the Mineralocorticoid Receptor, With Chronic Central Serous Chorioretinopathy.

JAMA ophthalmology - 1 May 2017

van Dijk Elon H C, Schellevis Rosa L, van Bergen Maaike G J M, Breukink Myrte B, Altay Lebriz, Scholz Paula, Fauser Sascha, Meijer Onno C, Hoyng Carel B, den Hollander Anneke I, Boon Camiel J F, de Jong Eiko K

Abstract excerpt

Importance: Chronic central serous chorioretinopathy (cCSC) is a chorioretinal disease with unknown disease etiology. The glucocorticoid receptor and the mineralocorticoid receptor, 2 glucocorticoid-binding receptors, might be involved in the pathogenesis of cCSC. Objective: To assess the association of functional variants and haplotypes in the glucocorticoid receptor (NR3C1) and mineralocorticoid receptor...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Single Nucleotide

Share to Receptors, Mineralocorticoid

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Source

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Identifiers

PMID: 28334414
DOI: 10.1001/jamaophthalmol.2017.0245
PMCID: PMC5847108

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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