OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect. (2018)

First Author: Thompson K

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.15252/emmm.201809060

PubMed Identifier: 30201738

Publication URI: http://europepmc.org/abstract/MED/30201738

Type: Journal Article/Review

Volume: 10

Parent Publication: EMBO molecular medicine

Issue: 11

ISSN: 1757-4676