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Common variants of EDA are associated with non-syndromic hypodontia.

Azza H Al-AniJoseph S AntounWilliam M ThomsonRuth ToplessTony R MerrimanMauro Farella
Published in: Orthodontics & craniofacial research (2020)
Common variants of the EDA genes are associated with specific phenotypes of non-syndromic hypodontia, thus confirming their role in the regulatory pathways of normal tooth development. However, larger samples are needed to investigate the association further.
Keyphrases
  • intellectual disability
  • copy number
  • genome wide
  • transcription factor
  • autism spectrum disorder
  • dna methylation
  • bioinformatics analysis
  • gene expression