Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome). (2009)
Attributed to:
Role of cytidine deaminases in epigenetic reprogramming and demethylation of DNA
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1371/journal.pgen.1000423
PubMed Identifier: 19300480
Publication URI: http://europepmc.org/abstract/MED/19300480
Type: Journal Article/Review
Volume: 5
Parent Publication: PLoS genetics
Issue: 3
ISSN: 1553-7390