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Novel alterations of CC2D1A as a candidate gene in a Turkish sample of patients with autism spectrum disorder.

Elif Funda SenerMuge Gulcihan OnalFatma DalUfuk NalbantogluYusuf OzkulHalit CanatanDidem Behice Oztop
Published in: The International journal of neuroscience (2020)
In vitro and in vivo functional analysis with this gene will help to understand its contribution to ASD pathogenesis. Future studies may help to elucidate the underlying biological mechanisms of these variants leading to the autism phenotype.
Keyphrases
  • autism spectrum disorder
  • copy number
  • intellectual disability
  • attention deficit hyperactivity disorder
  • genome wide
  • current status
  • genome wide analysis