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Article

PAX9 polymorphisms and susceptibility with sporadic tooth agenesis in Turkish populations: a case-control study.

BMC genomics - 26 Oct 2013

Isman Eren, Nergiz Suleyman, Acar Hasan, Sari Zafer

Abstract excerpt

BACKGROUND: Hypodontia, the congenital absence of one or a few teeth is one of the most common alterations of the human dentition. Familial hypodontia is caused by mutations in PAX9, Msx1 and Axin2 genes. Limited numbers of studies are present to show etiological factors beyond this anomaly in Turkish community belonging to Caucasian racial family. The purpose of this study is to investigate the relationships...

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Source

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Identifiers

PMID: 24160254
DOI: 10.1186/1471-2164-14-733
PMCID: PMC3826669

Genes

PAX9

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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