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7. Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy. Issue 2 (1st December 2020)

8. Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy. Issue 2 (1st December 2020)

9. Systematic analysis of a mitochondrial disease‐causing ND6 mutation in mitochondrial deficiency. Issue 5 (12th March 2020)