Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population.

BACKGROUND: Dental agenesis is the most common, often heritable, developmental anomaly in humans. Although WNT10A gene mutations are known to cause rare syndromes associated with tooth agenesis, including onycho-odontodermal dysplasia (OODD), Schöpf-Schulz-Passarge syndrome (SSPS), hypohidrotic ecto...

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Published in:	PLoS ONE
Main Authors:	Huiying He, Dong Han, Hailan Feng, Hong Qu, Shujuan Song, Baojing Bai, Zhenting Zhang
Format:	Article
Language:	English
Published:	Public Library of Science (PLoS) 2013-01-01
Online Access:	http://europepmc.org/articles/PMC3842385?pdf=render