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Article

Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars.

Archives of oral biology - 1 Jun 2012

Mostowska Adrianna, Biedziak Barbara, Jagodzinski Pawel P

Abstract excerpt

OBJECTIVE: Tooth agenesis is the most common developmental anomaly of the human dentition, with aetiology involving both genetic and environmental factors. The aim of the study was to search for casual mutations underlying hypodontia in a family with agenesis of the second premolars and third molars. DESIGN: Direct sequencing of the coding regions including exon-intron boundaries of the MSX1 and PAX9 genes was...

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Source

Identifiers

PMID: 22297032
DOI: 10.1016/j.archoralbio.2012.01.003

Genes

MSX1
PAX9

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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