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Article

A locus for autosomal dominant keratoconus maps to human chromosome 3p14–q13

1 Mar 2004

Abstract excerpt

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 14985379
DOI: 10.1136/jmg.2003.012872

Provenance

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Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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A locus for autosomal dominant keratoconus maps to human chromosome 3p14–q13PMID 14985379Read ↗

Genetics of Keratoconus: Where Do We Stand?Semantic proximity Read ↗

Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1.Semantic proximity Read ↗

A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.Semantic proximity Read ↗

Genetic and genomic perspective to understand the molecular pathogenesis of keratoconus.Semantic proximity Read ↗

A review of keratoconus: Diagnosis, pathophysiology, and genetics.Semantic proximity Read ↗

Resequencing of candidate genes for Keratoconus reveals a role for Ehlers–Danlos Syndrome genesSemantic proximity Read ↗

Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.Semantic proximity Read ↗

Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.Semantic proximity Read ↗

A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families.Semantic proximity Read ↗

The Genetics of Keratoconus: A ReviewSemantic proximity Read ↗

Update on the keratoconus genetics.Semantic proximity Read ↗

Genomic strategies to understand causes of keratoconus.Semantic proximity Read ↗

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