GeneticsEMBO ReportsPeer-reviewed
DNMT3B PWWP mutations cause hypermethylation of heterochromatin
Francesca Taglini, Ioannis Kafetzopoulos, Willow Rolls…·Duncan Sproul
This study shows that DNMT3B PWWP mutations cause hypermethylation of heterochromatin marked by H3K9me3, disrupting DNA methylation homeostasis and contributing to ICF syndrome, cancer, and aging.
20 citations