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 EderyPublished 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.