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Article

Common variants in the complement factor H gene confer genetic susceptibility to central serous chorioretinopathy.

Ophthalmology - 1 May 2014

Miki Akiko, Kondo Naoshi, Yanagisawa Suiho, Bessho Hiroaki, Honda Shigeru, Negi Akira

Abstract excerpt

PURPOSE: To investigate whether complement factor H (CFH) gene DNA variants are associated with central serous chorioretinopathy (CSCR). DESIGN: Cross-sectional study. PARTICIPANTS: A case-control group of 140 CSCR subjects and 2 different control groups: 934 population-based controls and 335 hospital-based controls. METHODS: Five single-nucleotide polymorphisms (SNPs) in CFH (rs3753394, rs800292, rs2284664,...

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Source

Identifiers

PMID: 24365176
DOI: 10.1016/j.ophtha.2013.11.020

Genes

CFH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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