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Article

Enamelin/ameloblastin gene polymorphisms in autosomal amelogenesis imperfecta among Syrian families.

Journal of investigative and clinical dentistry - 1 Feb 2011

Dashash Mayssoon, Bazrafshani Mohamed Riza, Poulton Kay, Jaber Saaed, Naeem Emad, Blinkhorn Anthony Stevenson

Abstract excerpt

AIM: This study was undertaken to investigate whether a single G deletion within a series of seven G residues (codon 196) at the exon 9-intron 9 boundary of the enamelin gene ENAM and a tri-nucleotide deletion at codon 180 in exon 7 (GGA vs deletion) of ameloblastin gene AMBN could have a role in autosomal amelogenesis imperfecta among affected Syrian families. METHODS: A new technique - size-dependent, deletion...

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Source

Identifiers

PMID: 25427323
DOI: 10.1111/j.2041-1626.2010.00038.x

Genes

ENAM
AMBN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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