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Article

A novel H572R mutation in the transforming growth factor-beta-induced gene in a Thai family with lattice corneal dystrophy type I.

Japanese journal of ophthalmology - 1 Jan 2000

Atchaneeyasakul La-Ongsri, Appukuttan Binoy, Pingsuthiwong Sarinee, Yenchitsomanus Pa-Thai, Trinavarat Adisak, Srisawat Chatchawan

Abstract excerpt

PURPOSE: To describe a large Thai family with lattice corneal dystrophy (LCD) type I and to determine whether this LCD is associated with mutations within the transforming growth factor-beta-induced (TGFBI) gene. METHODS: A six-generation family with LCD type I was identified and diagnosed on the basis of clinical and/or histopathologic evaluation. Visual acuity testing and slit-lamp biomicroscopic evaluation...

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Source

Identifiers

PMID: 17013691
DOI: 10.1007/s10384-006-0357-6

Genes

TGFBI

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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