📣 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.

Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhood. (2016)

First Author: Lewis-Smith D

Attributed to: Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/nxg.0000000000000059

PubMed Identifier: 27123478

Publication URI: http://europepmc.org/abstract/MED/27123478

Type: Journal Article/Review

Volume: 2

Parent Publication: Neurology. Genetics

Issue: 2

ISSN: 2376-7839