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Article

Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification.

European journal of human genetics : EJHG - 1 Apr 2015

de La Dure-Molla Muriel, Philippe Fournier Benjamin, Berdal Ariane

Abstract excerpt

Dentinogenesis imperfecta is an autosomal dominant disease characterized by severe hypomineralization of dentin and altered dentin structure. Dentin extra cellular matrix is composed of 90% of collagen type I and 10% of non-collagenous proteins among which dentin sialoprotein (DSP), dentin glycoprotein (DGP) and dentin phosphoprotein (DPP) are crucial in dentinogenesis. These proteins are encoded by a single...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 25118030
DOI: 10.1038/ejhg.2014.159
PMCID: PMC4666581

Genes

DSPP
DSP

Provenance

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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