A distinct mitochondrial myopathy, lactic acidosis and sideroblastic anemia (MLASA) phenotype associates with YARS2 mutations
Work
Year: 2013
Type: article
Abstract: ABSTRACT Nuclear‐encoded disorders of mitochondrial translation are clinically and genetically heterogeneous. Genetic causes include defects of mitochondrial aminoacyl‐tRNA synthetases, and factors re... more
Institutions MRC Mitochondrial Biology Unit, University College London, Great Ormond Street Hospital
Cites: 17
Cited by: 45
Related to: 10
FWCI: 3.588
Citation percentile (by year/subfield): 85.7
Subfield: Clinical Biochemistry
Domain: Life Sciences
Sustainable Development Goal Good health and well-being
Open Access status: hybrid