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Multiple Recurrent Copy Number Variations (CNVs) in Chromosome 22 Including 22q11.2 Associated with Autism Spectrum Disorder.

Safiah AlhazmiMaryam AlzahraniReem FarsiMona AlharbiKhloud AlgothmiNajla AlburaeMagdah GanashSheren AzhariFatemah BasingabAsma AlmuhammadiAmany I AlqosaibiHeba AlkhatabiAisha ElaimiMohammed JanHesham M AldhalaanAziza Rashed Al-RafiahAisha Alrofaidi
Published in: Pharmacogenomics and personalized medicine (2022)
CNV deletion and the duplication of the TBX1 gene could be related to ASD; therefore, this gene needs more analysis in terms of expression levels.
Keyphrases
  • copy number
  • mitochondrial dna
  • genome wide
  • poor prognosis
  • autism spectrum disorder
  • binding protein
  • intellectual disability
  • drug induced