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Background and objective.Mutations in the Leucine‐Rich Repeat Kinase 2 (LRRK2) gene at chromosome 12q12 are the most common genetic cause of sporadic and familial late‐onset Parkinson's disease. Our aim was to identify novel LRRK2 mutations in late‐onset Parkinson's disease families.
Design.We analyzed chromosome 12p11.2‐q13.1 haplotypes in 14 late‐onset Parkinson's disease families without known...
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