Complex I deficiency and Leigh syndrome through the eyes of a clinician

Karit Reinson; Katrin Õunap

doi:10.15252/emmm.202013187

EMBO Molecular Medicine (Oct 2020)

Complex I deficiency and Leigh syndrome through the eyes of a clinician

Karit Reinson,
Katrin Õunap

Affiliations

Karit Reinson: Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu
Katrin Õunap: Department of Clinical Genetics, Institute of Clinical Medicine, University of Tartu

DOI: https://doi.org/10.15252/emmm.202013187
Journal volume & issue: Vol. 12, no. 11
pp. 1 – 3

Abstract

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Graphical Abstract K. Õunap and K. Reinson discuss the biochemical and functional characterization of the NDUFC2 pathogenic variants identified in children with Leigh syndrome by R. Taylor and colleagues, in this issue of EMBO Molecular Medicine

Published in EMBO Molecular Medicine

ISSN: 1757-4676 (Print); 1757-4684 (Online)
Publisher: Springer Nature
Country of publisher: United Kingdom
LCC subjects: Medicine: Medicine (General); Science: Biology (General): Genetics
Website: https://www.embopress.org/journal/17574684

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