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A human pathology-related mutation prevents import of an aminoacyl-tRNA synthetase into mitochondria

  • M. Messmer
  • , C. Florentz
  • , H. Schwenzer
  • , G.C. Scheper
  • , M.S. van der Knaap
  • , L. Marechal-Drouard
  • , M. Sissler

    Research output: Contribution to JournalArticleAcademicpeer-review

    Abstract

    Mutations in the nuclear gene coding for the mitochondrial aspartyl-tRNA synthetase, a key enzyme for mitochondrial translation, are correlated with leukoencephalopathy. A Ser
    Original languageEnglish
    Pages (from-to)441-446
    JournalBiochemical Journal
    Volume433
    DOIs
    Publication statusPublished - 2011

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

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