📣 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.

Accelerating the genetic diagnosis of neurological disorders presenting with episodic apnoea in infancy. (2022)

First Author: Silksmith B

Attributed to: Exploring the role of neuromuscular excitability in sudden infant death funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/s2352-4642(22)00091-8

PubMed Identifier: 35525254

Publication URI: http://europepmc.org/abstract/MED/35525254

Type: Journal Article/Review

Volume: 6

Parent Publication: The Lancet. Child & adolescent health

Issue: 7

ISSN: 2352-4642