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Article

[Genetic, clinical and molecular analysis of a family affected by amelogenesis imperfecta].

Revista medica de Chile - 1 Nov 2005

Urzúa O Blanca, Ortega P Ana, Rodríguez M Luis, Morales B Irene

Abstract excerpt

BACKGROUND: Amelogenesis Imperfecta (AI) is a group of conditions where there is an abnormal formation of enamel in terms of quantity, structure and composition. AI is clinically and genetically heterogeneous, there are sex linked and autosomal versions, dominant and/or recessive, with phenotypes of hypoplastic, hypocalcified or hypomature enamel. Only recently, through clinical, genetic and molecular studies of...

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Source

Identifiers

PMID: 16446857
DOI: 10.4067/s0034-98872005001100009

Genes

AIDA
ENAM

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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