Leucine-rich repeat kinase 2 () c.6055G>A (p.G2019S) is a frequent cause of Parkinson's disease (PD), accounting for >30% of Tunisian Arab-Berber patients. is widely expressed in the immune system and its kinase activity confers a survival advantage against infection in animal models. Here, we assess haplotype variability and of the c.6055G>A mutation, define the age of the pathogenic allele, explore its relationship to the age of disease onset (AOO), and provide evidence for its positive selection.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11275506PMC
http://dx.doi.org/10.3390/genes15070878DOI Listing

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