Associated Papers
A de novo frameshift pathogenic variant in TBR1 identified in autism without intellectual disability.
Sapey-Triomphe LA et al.
Human Genomics, 2020
The TBR1-related autistic-spectrum-disorder phenotype and its clinical spectrum.
McDermott JH et al.
European Journal of Medical Genetics, 2018
De novo TBR1 mutations in sporadic autism disrupt protein functions.
Deriziotis P et al.
Nature Communications, 2014
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