📣 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.

Monoallelic loss-of-function THPO variants cause heritable thrombocytopenia. (2020)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1182/bloodadvances.2019001293

PubMed Identifier: 32150607

Publication URI: http://europepmc.org/abstract/MED/32150607

Type: Journal Article/Review

Volume: 4

Parent Publication: Blood advances

Issue: 5

ISSN: 2473-9529