📣 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.

Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number. (2023)

First Author: Pillalamarri V

Attributed to: UK Biobank (core renewal) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.xhgg.2022.100147

PubMed Identifier: 36311265

Publication URI: http://europepmc.org/abstract/MED/36311265

Type: Journal Article/Review

Volume: 4

Parent Publication: HGG advances

Issue: 1

ISSN: 2666-2477