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Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation. Cell metabolism, 2011/09/07, Volume 14, Issue 3, p.428-34, (2011)
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Systematic identification of human mitochondrial disease genes through integrative genomics. Nature genetics, 2006/05/01, Volume 38, Issue 5, p.576-82, (2006)
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