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Article

Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis.

European journal of medical genetics - 1 Aug 2016

Shahid Mohammad, Balto Hanan A, Al-Hammad Nouf, Joshi S, Khalil Hesham Saleh, Somily Ali Mohammed, Sinjilawi Nasr Abdul-Aziz, Al-Ghamdi Sameer, Faiyaz-Ul-Haque Muhammad, Dhillon Varinderpal S

Abstract excerpt

Tooth agenesis in human being is the most common congenital anomaly associated with dental development. Mutations in many genes such as MSH homeobox 1 (MSX1), paired box gene 9 (PAX9), ectodysplasin A (EDA) and EDA receptor (EDAR) have been associated with familial form of this condition. However, in large majority of patients, genetic cause could not be identified. The primary aim of present study was to...

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Source

Identifiers

PMID: 27365112
DOI: 10.1016/j.ejmg.2016.06.004

Genes

MSX1
PAX9
MMP20
EDA
EDAR

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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