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In the context of monogenic inheritance, the Leucine-rich repeat kinase 2 (LRRK2) gene is a prevalent pathogenic gene, with the Gly2019Ser mutation frequently observed in European, North African, and Jewish populations

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[DOI] [PMC free article] [PubMed] [Google Scholar] Hassan MI, Boosen M, Schaefer L, Kozlowska J, Eisel F, von Knethen A et al (2012)

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