Differential methylation of imprinting genes and MHC locus in 22q11.2 deletion syndrome-related schizophrenia spectrum disorders.
Miri CarmelElena MichaelovskyRonnie WeinbergerAmos FrischEhud Mekori-DomachevskyDoron GothelfAbraham WeizmanPublished in: The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry (2020)
The differential methylation in imprinting genes and in chr6p21-22 indicate the neurodevelopmental nature of 22q11.2DS-related SZ and the major role of MHC locus in the risk to develop SZ.