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Article

Common variants in the COL2A1 gene are associated with lattice degeneration of the retina in a Japanese population.

Molecular vision - 1 Jan 2019

Okazaki Shinya, Meguro Akira, Ideta Ryuichi, Takeuchi Masaki, Yonemoto Junichi, Teshigawara Takeshi, Yamane Takahiro, Okada Eiichi, Ideta Hidenao, Mizuki Nobuhisa

Abstract excerpt

Purpose: Lattice degeneration of the retina is a vitreoretinal disorder characterized by a visible fundus lesion that predisposes the patient to retinal detachment. It has been suggested that collagen type II alpha 1 (COL2A1) gene variants may contribute to the development of disorders associated with retinal detachment. Here we investigated whether COL2A1 gene variants were associated with the risk of lattice...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 31908402
PMCID: PMC6925665

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

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