Associated Papers
Drivers of Diagnostic Delay in Mitochondrial Disease: Missed Recognition of Canonical Features.
Tinker RJ et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.
Hagen CM et al.
Plos One, 2015
Identifying sequence variants in the human mitochondrial genome using high-resolution melt (HRM) profiling.
Dobrowolski SF et al.
Human Mutation, 2009
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