📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies. (2013)

First Author: Webb EA

Attributed to: MRC Wellcome Trust Human Developmental Biology Resource (HDBR) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awt218

PubMed Identifier: 24022475

Publication URI: http://europepmc.org/abstract/MED/24022475

Type: Journal Article/Review

Volume: 136

Parent Publication: Brain : a journal of neurology

Issue: Pt 10

ISSN: 0006-8950