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Article

Amelogenesis imperfecta.

Orphanet journal of rare diseases - 4 Apr 2007

Crawford Peter J M, Aldred Michael, Bloch-Zupan Agnes

Abstract excerpt

Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in origin, which affect the structure and clinical appearance of enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere...

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Source

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Identifiers

PMID: 17408482
DOI: 10.1186/1750-1172-2-17
PMCID: PMC1853073

Genes

AMELX
ENAM

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17408482-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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