Boczonadi, V.
King, M.S.
Smith, A.C.
Olahova, M.
Bansagi, B.
Roos, A.
Eyassu, F.
Borchers, C.
Ramesh, V.
Lochmüller, H.
Polvikoski, T.
Whittaker, R.G.
Pyle, A.
Griffin, H.
Taylor, R.W.
Chinnery, P.F.
Robinson, A.J.
Kunji, E.R.S.
Horvath, R.
This article is maintained by: Elsevier
Article Title: Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0506-1
CrossRef DOI link to the associated document: https://doi.org/10.1038/gim.2017.251
Content Type: article
Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics