Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson’s disease

Overview of attention for article published in Brain, December 2022

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Trinh et al. report that PINK1/PRKN mutations predispose individuals to mitochondrial DNA variant accumulation in a dose- and disease-dependent manner. https://t.co/5pMiTSVFGk https://t.co/wpJEjJq7sh

RT @Brain1878: Trinh et al. report that PINK1/PRKN mutations predispose individuals to mitochondrial DNA variant accumulation in a dose- an…

Trinh et al. report that PINK1/PRKN mutations predispose individuals to mitochondrial DNA variant accumulation in a dose- and disease-dependent manner. https://t.co/g7i9qsZXVp https://t.co/Uz47P5Xwim

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