期刊论文详细信息
Molecular Genetics & Genomic Medicine
Mutations in the mitochondrial tryptophanyl‐tRNA synthetase cause growth retardation and progressive leukoencephalopathy
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[1] Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy;Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden;Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden;Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden;Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden;Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden;Max Planck Institute Biology of Ageing ‐ Karolinska Institutet Laboratory, Stockholm, Sweden;Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden;Max Planck Institute Biology of Ageing ‐ Karolinska Institutet Laboratory, Stockholm, Sweden;Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden;Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden;Max Planck Institute Biology of Ageing ‐ Karolinska Institutet Laboratory, Stockholm, Sweden;Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden;Max Planck Institute Biology of Ageing ‐ Karolinska Institutet Laboratory, Stockholm, Sweden;Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden;Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden;
关键词: aminoacylation;    mitochondria;    mitochondrial tryptophanyl‐tRNA synthetase;    WARS2;   
DOI  :  10.1002/mgg3.654
来源: publisher
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