Frequency of Heterozygous Parkin (PRKN) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort

Overview of attention for article published in Frontiers in Neurology, August 2021

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In the top 25% of all research outputs scored by Altmetric
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New article: Frequency of Heterozygous Parkin (PRKN) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort https://t.co/u0chvnlAjP #parkinsons #neurology https://t.co/RK8FuuqvPF

RT @EuracBiomed: 🧠#PRKN gene mutations cause autosomal recessive #Parkinson’s disease. Since there are many carriers of PRKN mutations, it’…

RT @EuracBiomed: 🧠#PRKN gene mutations cause autosomal recessive #Parkinson’s disease. Since there are many carriers of PRKN mutations, it’…

RT @FrontNeurol: New Research: Frequency of Heterozygous Parkin (PRKN) Variants and Penetrance of Parkinson's Disease Risk Markers in the P…

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