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Article

A model of FAS1 domain 4 of the corneal protein beta(ig)-h3 gives a clearer view on corneal dystrophies.

Molecular vision - 11 Sept 2003

Clout Naomi J, Hohenester Erhard

Abstract excerpt

PURPOSE: A progressive alteration of the cornea resulting in loss of transparency occurs in a set of hereditary diseases known as corneal dystrophies. A number of these dystrophies have been linked to mutations in the 5q31-linked gene product beta(ig)-h3 (TGFBIP, kerato-epithelin, MP78/70, RGD-CAP) although the mechanism by which the mutations cause disease remains unknown. Here we investigate the structural...

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Share to Cell Adhesion Molecules, Neuronal
Share to Chromosomes, Human, Pair 5
Share to Cornea

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Corneal Dystrophies, Hereditary

Share to Extracellular Matrix Proteins

Share to Molecular Structure

Share to Protein Interaction Mapping

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Source

Identifiers

PMID: 14502125

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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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