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1. Genome sequencing reanalysis increases the diagnostic yield in dystonia

5. Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants

6. The commercial genetic testing landscape for Parkinson's disease

7. Mitochondrial disease in adults: recent advances and future promise

9. The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease

10. Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes

14. Expanding the spectrum of PEX16 mutations and novel insights into disease mechanisms

15. Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

19. LARS2 variations can cause lethal infantile multisystem failure

21. 63.

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49. Mitochondrial DNA abnormalities and autistic spectrum disorders

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