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At least seven mutations in LRRK2 are known to be pathogenic based upon clear segregation with disease in LRRK2 -linked families, including N1437H, R1441C/G/H, Y1699C, G2019S and I2020T, with G2019S representing the most frequent mutation [812]

Neurotherapeutics 16 , 11331148 (2019)

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