Associated Papers
Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome.
Weerts MJA et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
De novo variants in SETD1B cause intellectual disability, autism spectrum disorder, and epilepsy with myoclonic absences.
Hiraide T et al.
Epilepsia Open, 2019
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