The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype. (2011)

First Author: Cross SH
Attributed to:  Genetic models of human disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddq457

PubMed Identifier: 20943750

Publication URI: http://europepmc.org/abstract/MED/20943750

Type: Journal Article/Review

Volume: 20

Parent Publication: Human molecular genetics

Issue: 2

ISSN: 0964-6906