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Article

Molecular-based phenotype variations in amelogenesis imperfecta.

Oral diseases - 1 Sept 2023

Dong Jing, Ruan Wenyan, Duan Xiaohong

Abstract excerpt

Amelogenesis imperfecta (AI) is one of the typical dental genetic diseases in human. It can occur isolatedly or as part of a syndrome. Previous reports have mainly clarified the types and mechanisms of nonsyndromic AI. This review aimed to compare the phenotypic differences among the hereditary enamel defects with or without syndromes and their underlying pathogenic genes. We searched the articles in PubMed with...

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Identifiers

PMID: 37154292
DOI: 10.1111/odi.14599

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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