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Targeted exome sequencing of suspected mitochondrial disorders. Neurology, 2013/05/07, Volume 80, Issue 19, p.1762-1770, (2013)
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Evolutionary diversity of the mitochondrial calcium uniporter. Science (New York, N.Y.), 2012/05/18, Volume 336, Issue 6083, p.886, (2012)
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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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The mitochondrial proteome and human disease. Annual review of genomics and human genetics, 2010/09/22, Volume 11, p.25-44, (2010)
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Genomic analysis of the basal lineage fungus Rhizopus oryzae reveals a whole-genome duplication. PLoS genetics, 2009/07/01, Volume 5, Issue 7, p.e1000549, (2009)
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Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans. Proceedings of the National Academy of Sciences of the United States of America, 2009/05/05, Volume 106, Issue 18, p.7507-12, (2009)
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A mitochondrial protein compendium elucidates complex I disease biology. Cell, 2008/07/11, Volume 134, Issue 1, p.112-23, (2008)
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Sequencing of Aspergillus nidulans and comparative analysis with A. fumigatus and A. oryzae. Nature, 2005/12/22, Volume 438, Issue 7071, p.1105-15, (2005)
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