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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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Am J Hum Genet
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2016
Aiheet:
Report
Linkit: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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