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Article

A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32.

Investigative ophthalmology & visual science - 1 Sept 2006

Sundin Olof H, Broman Karl W, Chang Howard H, Vito Elizabeth C L, Stark Walter J, Gottsch John D

Abstract excerpt

PURPOSE: To identify the genetic basis of late-onset Fuchs corneal dystrophy (FCD). METHODS: Phenotypes and genotypes at 1107 short tandem repeat polymorphism markers were obtained for 43 affected and 33 unaffected individuals in three large families. Two-point genetic linkage analysis was performed with MLINK and multipoint linkage with SimWalk 2.89. RESULTS: In each family, the most significant cluster of...

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Source

Identifiers

PMID: 16936105
DOI: 10.1167/iovs.05-1619

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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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