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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Detalles Bibliográficos
Autores principales: He, Huiying, Han, Dong, Feng, Hailan, Qu, Hong, Song, Shujuan, Bai, Baojing, Zhang, Zhenting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842385/
https://www.ncbi.nlm.nih.gov/pubmed/24312213
http://dx.doi.org/10.1371/journal.pone.0080393

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842385/
https://www.ncbi.nlm.nih.gov/pubmed/24312213
http://dx.doi.org/10.1371/journal.pone.0080393

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