Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup
出版年份 2013 全文链接
标题
Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup
作者
关键词
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出版物
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 110, Issue 9, Pages 3453-3458
出版商
Proceedings of the National Academy of Sciences
发表日期
2013-02-12
DOI
10.1073/pnas.1300690110
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- Mitochondrial Energetics and Therapeutics
- (2010) Douglas C. Wallace et al. Annual Review of Pathology-Mechanisms of Disease
- Multiplex analysis of mitochondrial DNA pathogenic and polymorphic sequence variants
- (2010) Jason C. Poole et al. BIOLOGICAL CHEMISTRY
- Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny
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