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

18 Citations (Scopus)

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
Issue number3
DOIs
Publication statusPublished - 2011

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