Targeted next-generation sequencing expands the spectrum of mitochondrial disorders

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Si Houn Hahn
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[1] University of Washington School of Medicine,Department of Pediatrics, Division of Genetic Medicine
[2] Seattle Children's Hospital,undefined
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Heterogeneity; mitochondria; mitochondrial disorders; mutations; next-generation sequencing;
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摘要
Next-generation sequencing has become a powerful tool for testing genetically and clinically heterogeneous conditions such as mitochondrial disorders. A recent study published in Science Translational Medicine underscores the considerable clinical benefits of targeted next-generation sequencing for the diagnosis of mitochondrial disorders. The findings also suggest that the genetic heterogeneity that can result in mitochondrial disease appears much broader than previously thought.
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