Condition: MENTAL RETARDATION, AUTOSOMAL DOMINANT 58


rs1554776500 in SET gene and MENTAL RETARDATION, AUTOSOMAL DOMINANT 58 PMID 29688601 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.

PMID 25356899 2014 De novo mutations in moderate or severe intellectual disability.