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Article

Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia.

Archives of oral biology - 1 Aug 2008

Xuan Kun, Jin Fang, Liu Yan-Li, Yuan Lin-Tian, Wen Ling-Ying, Yang Fu-Sheng, Wang Xiao-Jing, Wang Guo-Hua, Jin Yan

Abstract excerpt

OBJECTIVES: Oligodontia is defined as the congenital absence of 6 or more permanent teeth excluding the third molar. The occurrence of non-syndromic still remains poorly understood, but in recent years some cases have been reported where mutations or polymorphisms of PAX9 and MSX1 had been associated with non-syndromic oligodontia. The objective of the present work was to study the phenotype and genotype of three...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18374898
DOI: 10.1016/j.archoralbio.2008.02.012

Genes

MSX1
PAX9

Variants

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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