📣 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.

Age-dependent epileptic encephalopathy associated with an unusual co-occurrence of ZEB2 and SCN1A variants. (2020)

First Author: Nardello R

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/10.1684/epd.2020.1138

PubMed Identifier: 32031527

Publication URI: http://europepmc.org/abstract/MED/32031527

Type: Journal Article/Review

Volume: 22

Parent Publication: Epileptic disorders : international epilepsy journal with videotape

Issue: 1

ISSN: 1294-9361