SET

Publications

Stevens SJ et al. 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. Hum Mutat. 2018;39(7):1014-1023. PMID: 29688601.

Richardson R et al. SET de novo frameshift variants associated with developmental delay and intellectual disabilities. Eur J Hum Genet. 2018; 26(9):1306-1311. PMID: 29907757.

Hamdan FF et al. De novo mutations in moderate or severe intellectual disability. PLoS Genet. 2014; 10(10):e1004772. PMID: 25356899.