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Article

CFI-rs7356506 polymorphisms associated with Vogt-Koyanagi-Harada syndrome.

Molecular vision - 1 Jan 2016

Dai Ma-Li, Huang Xiu-Feng, Wang Qing-Feng, Cai Wei-Jun, Jin Zi-Bing, Wang Yuqin

Abstract excerpt

PURPOSE: Complement factor I (CFI) plays an important role in complement activation pathways and is known to affect the development of uveitis. The present study was performed to investigate the existence of an association between CFI genetic polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome. METHODS: A total of 100 patients diagnosed with VKH syndrome and 300 healthy controls were recruited for the study....

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Source

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Identifiers

PMID: 26900322
PMCID: PMC4734154

Genes

CFI

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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