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Neurodegenerative disease-associated mutants of a human mitochondrial aminoacyl-tRNA synthetase present individual molecular signatures
Mutations in human mitochondrial aminoacyl-tRNA synthetases are associated with a variety of neurodegenerative disorders. The effects of these mutations on the structure and function of the enzymes remain to be established. Here, we investigate six mutants of the aspartyl-tRNA synthetase correlated...
Autores principales: | Sauter, Claude, Lorber, Bernard, Gaudry, Agnès, Karim, Loukmane, Schwenzer, Hagen, Wien, Frank, Roblin, Pierre, Florentz, Catherine, Sissler, Marie |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664897/ https://www.ncbi.nlm.nih.gov/pubmed/26620921 http://dx.doi.org/10.1038/srep17332 |
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