📣 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.

Biallelic variants in SLC38A3 encoding a glutamine transporter cause epileptic encephalopathy. (2022)

First Author: Marafi D

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/10.1093/brain/awab369

PubMed Identifier: 34605855

Publication URI: http://europepmc.org/abstract/MED/34605855

Type: Journal Article/Review

Volume: 145

Parent Publication: Brain : a journal of neurology

Issue: 3

ISSN: 0006-8950