Associated Papers
Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder.
Bacchelli E et al.
Research Square, 2023
Case report: A novel frameshift mutation in BRSK2 causes autism in a 16-year old Chinese boy.
Hu Y et al.
Frontiers in Psychiatry, 2023
37671287 (PubMed )
Supplement: Table_1.XLSX › Sheet1
Deleterious Variation in BR Serine/Threonine Kinase 2 Classified a Subtype of Autism.
Deng J et al.
Frontiers in Molecular Neuroscience, 2022
Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.
Hiatt SM et al.
American Journal of Human Genetics, 2019
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