Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency
出版年份 2016 全文链接
标题
Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency
作者
关键词
<em class=EmphasisTypeItalic >WNT10A</em> mutations, Ectodermal dysplasia, Dental, Primary dentition, Permanent dentition
出版物
BMC Medical Genetics
Volume 17, Issue 1, Pages -
出版商
Springer Nature
发表日期
2016-11-24
DOI
10.1186/s12881-016-0349-4
参考文献
相关参考文献
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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- Common polymorphisms in WNT10A affect tooth morphology as well as hair shape
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- Mutations inWNT10Aare frequently involved in oligodontia associated with minor signs of ectodermal dysplasia
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- WNT10Amutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations
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- Candidate Gene Analysis of Tooth Agenesis Identifies Novel Mutations in Six Genes and Suggests Significant Role for WNT and EDA Signaling and Allele Combinations
- (2013) Sirpa Arte et al. PLoS One
- Wnt/β-Catenin Signaling and Disease
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- Tooth shape formation and tooth renewal: evolving with the same signals
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