A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation. (2019)
Attributed to:
A Systems Approach to Understanding Methylation Programming in Oocytes and its Consequences in Development
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1186/s13073-019-0694-y
PubMed Identifier: 31847873
Publication URI: http://europepmc.org/abstract/MED/31847873
Type: Journal Article/Review
Volume: 11
Parent Publication: Genome medicine
Issue: 1
ISSN: 1756-994X