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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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發表在: | Am J Hum Genet |
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Main Authors: | , , , , , , , , , , , , , , , |
格式: | Artigo |
語言: | Inglês |
出版: |
Elsevier
2016
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主題: | |
在線閱讀: | 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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