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Article

A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.

Archives of oral biology - 1 Jul 2014

Abdalla Ebtesam M, Mostowska Adrianna, Jagodziński Paweł P, Dwidar Karin, Ismail Suzan R

Abstract excerpt

OBJECTIVE: Tooth agenesis is the most common dental anomaly, whose aetiology still remains to be fully elucidated. The aim of this study was to investigate the genetic cause of non-syndromic hypodontia with clinical variability in an Egyptian family. DESIGN: The entire coding regions including exon-intron boundaries of the MSX1, PAX9 and WNT10A genes were investigated by direct sequencing in all affected family...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 24798981
DOI: 10.1016/j.archoralbio.2014.04.004

Genes

MSX1
PAX9

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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