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Article

Leu518Pro mutation of the βig-h3 gene causes lattice corneal dystrophy type I

1 Jul 1999

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Share to Connective tissue disorders research
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 10482106
DOI: 10.1016/s0002-9394(99)00053-7

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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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Leu518Pro mutation of the βig-h3 gene causes lattice corneal dystrophy type IPMID 10482106Read ↗

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