Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease (vol 20, pg 1224, 2018): 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)

V. Boczonadi, M. S. King, A. C. Smith, M. Olahova, B. Bansagi, A. Roos, F. Eyassu, C. Borchers, V. Ramesh, H. Lochmüller, T. Polvikoski, R. G. Whittaker, A. Pyle, H. Griffin, R. W. Taylor, P. F. Chinnery, A. J. Robinson, E. R.S. Kunji, R. Horvath

Research output: Contribution to journalComment/debate

Abstract

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Original languageEnglish
Pages (from-to)2163-2164
Number of pages2
JournalGenetics in Medicine
Volume21
Issue number9
DOIs
Publication statusPublished - 1 Sep 2019
Externally publishedYes

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