A novel mutation in YARS2 causes myopathy with lactic acidosis and sideroblastic anemia
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Title
A novel mutation in YARS2 causes myopathy with lactic acidosis and sideroblastic anemia
Authors
Keywords
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Journal
HUMAN MUTATION
Volume 33, Issue 8, Pages 1201-1206
Publisher
Wiley
Online
2012-04-14
DOI
10.1002/humu.22098
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- Mitochondrial DNA mutations and human disease
- (2009) Helen A.L. Tuppen et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome
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- Aminoacyl tRNA synthetases and their connections to disease
- (2008) S. G. Park et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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