📣 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.

Paediatric single mitochondrial DNA deletion disorders: an overlapping spectrum of disease. (2015)

First Author: Broomfield A

Attributed to: MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s10545-014-9778-4

PubMed Identifier: 25352051

Publication URI: http://europepmc.org/abstract/MED/25352051

Type: Journal Article/Review

Volume: 38

Parent Publication: Journal of inherited metabolic disease

Issue: 3

ISSN: 0141-8955