Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families
出版年份 2016 全文链接
标题
Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families
作者
关键词
-
出版物
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 24, Issue 10, Pages 1430-1435
出版商
Springer Nature
发表日期
2016-04-06
DOI
10.1038/ejhg.2016.29
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia
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- Context-Dependent Activation or Inhibition of Wnt- -Catenin Signaling by Kremen
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- Wnt/β-catenin signaling directs multiple stages of tooth morphogenesis
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