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Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genome.
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has major subject area list
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Exome; Genome, Mitochondrial; Mitochondrial Diseases; Sequence Analysis, RNA
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has minor subject area list
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Ataxia; Child, Preschool; Electron Transport Complex I; Female; Genetic Variation; Heterozygote; High-Throughput Nucleotide Sequencing; Humans; Infant; Infant, Newborn; Leigh Disease; Mitochondria; Molecular Diagnostic Techniques; Muscle Weakness; Pedigree; Sequence Analysis, DNA; Ubiquinone
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