Barely Significant
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Rare variants in LRRK1 and Parkinson's disease.

Neurogenetics · 2014 · PMC3968516 · PMID 24241507

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showed a trendno p-value reported
Tunisian individuals with LRRK2 p.Gly2019Ser showed a trend towards a 6-year earlier age of onset when they also carried LRRK1 p.Leu416Met [ 20 ].

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