📣 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.

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype. (2016)

First Author: Toubiana J
Attributed to:  MRC Centre for Medical Mycology funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1182/blood-2015-11-679902

PubMed Identifier: 27114460

Publication URI: http://europepmc.org/abstract/MED/27114460

Type: Journal Article/Review

Volume: 127

Parent Publication: Blood

Issue: 25

ISSN: 0006-4971