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Article

Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping.

Human genetics - 1 Dec 1997

Laass M W, Hennies H C, Preis S, Stevens H P, Jung M, Leigh I M, Wienker T F, Reis A

Abstract excerpt

Papillon-Lefèvre syndrome is an autosomal recessively inherited palmoplantar keratoderma of unknown aetiology associated with severe periodontitis leading to premature loss of dentition. Three consanguineous families, two of Turkish and one of German origin, and three multiplex families, one of E...

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Identifiers

PMID: 9439671
DOI: 10.1007/s004390050645

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-9439671-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping.PMID 9439671Read ↗

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

Sublocalization of the Papillon-Lefevre syndrome locus on 11q14-q21Semantic proximity Read ↗

Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome.Semantic proximity Read ↗

Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation.Semantic proximity Read ↗

A genetic study of cathepsin C gene in two families with Papillon-Lefèvre syndrome.Semantic proximity Read ↗

Partial expression of the Papillon-Lefèvre syndrome in 2 unrelated families.Semantic proximity Read ↗

Cathepsin-C (CTSC) Gene Mutations in Papillon-Lefevre Syndrome in India.Semantic proximity Read ↗

Phenotypic variation and allelic heterogeneity in young patients with Papillon-Lefèvre syndrome.Semantic proximity Read ↗

Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the LiteratureSemantic proximity Read ↗

Papillon-Lefèvre syndrome with homozygous nonsense mutation of cathepsin C gene presenting with late-onset periodontitis.Semantic proximity Read ↗

Identification of cathepsin C mutations in ethnically diverse papillon-Lefèvre syndrome patients.Semantic proximity Read ↗

Papillon-Lefevre syndrome: Report of two cases in the same familySemantic proximity Read ↗

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