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

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18 Citations (Scopus)


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
Issue number3
Publication statusPublished - 2011

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