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Article

An Arg124Cys mutation in transforming growth factor β-induced gene associated with lattice corneal dystrophy type I in a Chinese pedigree.

Indian journal of ophthalmology - 1 Jan 2022

Li Feng, He Jiahuan, Bai Hua, Huang Yifei, Wang Fang, Tian Lei

Abstract excerpt

PURPOSE: To identify a clinical and genetic form of a large Chinese family with an autosomal-dominant lattice corneal dystrophy type I (LCD I). METHODS: The patients' eyes were examined on the basis of slit-lamp microscopy, and other clinical records were also collected. Genomic DNA was extracted from peripheral leukocytes of the affected patients and their unaffected family members. Each previous reported...

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Identifiers

PMID: 34937214
DOI: 10.4103/ijo.IJO_33_21
PMCID: PMC8917566

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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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