📣 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.

Genetic variation in NFE2L2 is associated with outcome following aneurysmal subarachnoid haemorrhage (2022)

First Author: Gaastra B

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/ene.15571

PubMed Identifier: 36148820

Publication URI: http://europepmc.org/abstract/MED/36148820

Type: Journal Article/Review

Parent Publication: European Journal of Neurology

Issue: 1

ISSN: 1351-5101