📣 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.

Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance. (2014)

First Author: Pfeffer G

Attributed to: CIMA: The Centre for Integrated Research into Musculoskeletal Ageing funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awu060

PubMed Identifier: 24727571

Publication URI: http://europepmc.org/abstract/MED/24727571

Type: Journal Article/Review

Volume: 137

Parent Publication: Brain : a journal of neurology

Issue: Pt 5

ISSN: 0006-8950