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Article

The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.

Molecular vision - 17 Sept 2007

Correa-Gomez Vicente, Villalvazo-Cordero Leonardo, Zenteno Juan Carlos

Abstract excerpt

PURPOSE: To report the clinical, molecular, and histopathological features of a distinct transforming growth factor-beta-induced (TGFBI) gene-linked amyloidotic corneal dystrophy exhibiting an unusual lattice pattern. METHODS: A complete ophthalmologic examination was performed in 10 individuals...

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Source

Identifiers

PMID: 17893671

Genes

TGFBI

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17893671-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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