Use of stereotypical mutational motifs to define resolution limits for the ultra-deep resequencing of mitochondrial DNA. [electronic resource]
Producer: 20151022Description: 413-5 p. digitalISSN:- 1476-5438
- Case-Control Studies
- DNA, Mitochondrial -- genetics
- High-Throughput Nucleotide Sequencing -- standards
- Humans
- Intestinal Pseudo-Obstruction -- diagnosis
- Mitochondrial Encephalomyopathies -- diagnosis
- Muscular Dystrophy, Oculopharyngeal
- Mutation
- Nucleotide Motifs
- Ophthalmoplegia -- congenital
- Sensitivity and Specificity
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Publication Type: Journal Article
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