Mitochondria: Impaired mitochondrial translation in human disease
2014 · The International Journal of Biochemistry & Cell Biology · 189 citations
https://doi.org/10.1016/j.biocel.2013.12.011
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Veronika Boczonadi
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Veronika Boczonadi is an academic researcher from Newcastle University. The author has contributed to research in topics: Mitochondrial Function and Pathology & Metabolism and Genetic Disorders & RNA modifications and cancer. The author has an h-index of 23, co-authored 40 publications.
Papers by this author
worksANO10 mutations cause ataxia and coenzyme Q10 deficiency
2014 · Journal of Neurology · 83 citations
https://doi.org/10.1007/s00415-014-7476-7
Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease
2018 · Genetics in Medicine · 59 citations
https://doi.org/10.1038/gim.2017.251
Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease
2019 · Genetics in Medicine · 2 citations
https://doi.org/10.1038/s41436-019-0506-1
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