Mutations in WNT10B Are Identified in Individuals with Oligodontia

Tooth agenesis is one of the most common developmental anomalies in humans. Oligodontia, a severe form of tooth agenesis, is genetically and phenotypically a heterogeneous condition. Although significant efforts have been made, the genetic etiology of dental agenesis remains largely unknown. In the...

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Dades bibliogràfiques
Publicat a:Am J Hum Genet
Autors principals: Yu, Ping, Yang, Wenli, Han, Dong, Wang, Xi, Guo, Sen, Li, Jinchen, Li, Fang, Zhang, Xiaoxia, Wong, Sing-Wai, Bai, Baojing, Liu, Yao, Du, Jie, Sun, Zhong Sheng, Shi, Songtao, Feng, Hailan, Cai, Tao
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2016
Matèries:
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5005437/
https://ncbi.nlm.nih.gov/pubmed/27321946
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2016.05.012
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