DNMT3B PWWP mutations cause hypermethylation of heterochromatin. (2024)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s44319-024-00061-5

PubMed Identifier: 38291337

Publication URI: http://europepmc.org/abstract/MED/38291337

Type: Journal Article/Review

Parent Publication: EMBO reports

ISSN: 1469-221X