Lastly, some variants were present in all lines, with varying heteroplasmy levels following a clear trend (e.g., m.310T > C, lower in AT1 than REBL-PAT and HUES7—potentially protective; m.310_311insC, higher in AT1 than REBL-PAT and HUES7—likely aggravator).
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Mitochondrial DNA: Hotspot for Potential Gene Modifiers Regulating Hypertrophic Cardiomyopathy.
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