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Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease (Genetics in Medicine, (2018), 20, 10, (1224-1235), 10.1038/gim.2017.251)

Lookup NU author(s): Dr Veronika Boczonadi, Dr Monika Olahova, Dr Boglárka Bánsági, Dr Andreas Roos, Dr Vankateswara Ramesh, Professor Hanns Lochmuller, Dr Tuomo Polvikoski, Dr Roger Whittaker, Dr Angela Pyle, Dr Helen Griffin, Professor Robert Taylor, Professor Patrick Chinnery, Professor Rita Horvath

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

© 2019, The Author(s). This Article was originally published under Nature Research’s License to Publish, but has now been made available under a [CC BY 4.0] license. The PDF and HTML versions of the Article have been modified accordingly.


Publication metadata

Author(s): Boczonadi V, King MS, Smith AC, Olahova M, Bansagi B, Roos A, Eyassu F, Borchers C, Ramesh V, Lochmuller H, Polvikoski T, Whittaker RG, Pyle A, Griffin H, Taylor RW, Chinnery PF, Robinson AJ, Kunji ERS, Horvath R

Publication type: Note

Publication status: Published

Journal: Genetics in Medicine

Year: 2019

Pages: Epub ahead of print

Online publication date: 26/04/2019

Acceptance date: 02/04/2018

ISSN (print): 1098-3600

ISSN (electronic): 1530-0366

Publisher: Nature Publishing Group

URL: https://doi.org/10.1038/s41436-019-0506-1

DOI: 10.1038/s41436-019-0506-1


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