Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome). (2009)

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