📣 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.

Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stability. (2023)

First Author: Erdinc D

Attributed to: Pleiotropic disorders of mitochondrial translation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.15252/emmm.202216775

PubMed Identifier: 37013609

Publication URI: http://europepmc.org/abstract/MED/37013609

Type: Journal Article/Review

Volume: 15

Parent Publication: EMBO molecular medicine

Issue: 5

ISSN: 1757-4676