Mutations in the NHEJ component XRCC4 cause primordial dwarfism. (2015)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2015.01.013

PubMed Identifier: 25728776

Publication URI: http://europepmc.org/abstract/MED/25728776

Type: Journal Article/Review

Volume: 96

Parent Publication: American journal of human genetics

Issue: 3

ISSN: 0002-9297