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Article

Linkage of posterior polymorphous corneal dystrophy to 20q11

1 Jan 1995

Abstract excerpt

Posterior polymorphous dystrophy (PPMD) is an autosomal dominant disorder of the cornea that is clinically recognized by the presence of vesicles on the endothelial surface of the cornea. The corneal endothelium is normally a single layer of cells that lose their mitotic potential after development is complete. In PPMD, the endothelium is often multi-layered and has several other characteristics of an epithelium...

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Identifiers

PMID: 7795607
DOI: 10.1093/hmg/4.3.485

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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.

Related research

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

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Linkage of posterior polymorphous corneal dystrophy to 20q11PMID 7795607Read ↗

A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10.Semantic proximity Read ↗

High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation.Semantic proximity Read ↗

Posterior Polymorphous Corneal Dystrophy in Czech Families Maps to Chromosome 20 and Excludes the<i>VSX1</i>GeneSemantic proximity Read ↗

Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.Semantic proximity Read ↗

Genetic analysis of chromosome 20-related posterior polymorphous corneal dystrophy: genetic heterogeneity and exclusion of three candidate genes.Semantic proximity Read ↗

Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval.Semantic proximity Read ↗

The utility of next-generation sequencing in the evaluation of the posterior polymorphous corneal dystrophy 1 locus.Semantic proximity Read ↗

Identification of Potentially Pathogenic Variants in the Posterior Polymorphous Corneal Dystrophy 1 Locus.Semantic proximity Read ↗

Two-stage genome-wide linkage scan in keratoconus sib pair families.Semantic proximity Read ↗

Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED loci.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 ↗

Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 region.Semantic proximity Read ↗

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