Associated Papers
Whole exome sequencing and transcriptome analysis in two unrelated patients with novel SET mutations.
Pan X et al.
Journal of Human Genetics, 2023
SET de novo frameshift variants associated with developmental delay and intellectual disabilities.
Richardson R et al.
European Journal of Human Genetics : Ejhg, 2018
De novo mutations in the SET nuclear proto-oncogene, encoding a component of the inhibitor of histone acetyltransferases (INHAT) complex in patients with nonsyndromic intellectual disability.
Stevens SJC et al.
Human Mutation, 2018
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