📣 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.

Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study. (2021)

First Author: Schon KR

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/10.1136/bmj-2021-066288

PubMed Identifier: 34732400

Publication URI: http://europepmc.org/abstract/MED/34732400

Type: Journal Article/Review

Volume: 375

Parent Publication: BMJ (Clinical research ed.)

ISSN: 0959-8138