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Article

Molecular basis of human dentin diseases.

American journal of medical genetics. Part A - 1 Dec 2006

MacDougall Mary, Dong Juan, Acevedo Ana Carolina

Abstract excerpt

In recent years, substantial progress has been made regarding the molecular etiology of human structural tooth diseases that alter dentin matrix formation. These diseases have been classified into two major groups with subtypes: dentin dysplasia (DD) types I and II and dentinogenesis imperfecta (DGI) types I-III. Genetic linkage studies have identified the critical loci for DD-II, DGI-II, and DGI-II to human...

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Source

Identifiers

PMID: 16955410
DOI: 10.1002/ajmg.a.31359

Genes

DMP1
DSPP
MEPE

Provenance

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.

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