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A de novo frameshift pathogenic variant in TBR1 identified in autism without intellectual disability.

Laurie-Anne Sapey-TriompheJulie ReversatGaëtan LescaNicolas ChatronMarina BussaSylvie MazoyerChristina SchmitzSandrine SoniéPatrick Edery
Published in: Human genomics (2020)
Based on this case report, we discuss the role of TBR1 in general brain development, language development, intellectual disability and other symptoms of ASD. Providing a detailed clinical description of the individuals with such pathogenic variants should help to understand the genotype-phenotype relationships in ASD.
Keyphrases
  • intellectual disability
  • autism spectrum disorder
  • case report
  • attention deficit hyperactivity disorder
  • copy number
  • white matter
  • resting state
  • subarachnoid hemorrhage
  • genome wide