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MFN2 mutations cause compensatory mitochondrial DNA proliferation.

Published version
Peer-reviewed

Repository URI

https://www.repository.cam.ac.uk/handle/1810/290366

Repository DOI

https://doi.org/10.17863/CAM.37596
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Published version (134.11 KB)

Type

Article

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Authors

Description

Keywords

DNA, Mitochondrial, Female, GTP Phosphohydrolases, Humans, Male, Mitochondrial Myopathies, Mitochondrial Proteins, Optic Atrophy

Journal Title

Brain

Conference Name

Journal ISSN

0006-8950
1460-2156

Volume Title

135

Publisher

Oxford University Press (OUP)

Publisher DOI

https://doi.org/10.1093/brain/aws049

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Attribution-NonCommercial 4.0 International
Except where otherwised noted, this item's license is described as Attribution-NonCommercial 4.0 International

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University of Cambridge Research Outputs (Articles and Conferences)