MFN2 mutations cause compensatory mitochondrial DNA proliferation.
Published version
Peer-reviewed
Repository URI
Repository DOI
Change log
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
1460-2156
Volume Title
135
Publisher
Oxford University Press (OUP)