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Nathan Pankratz, Michael W. Pauciulo, Veronika E. Elsaesser, Diane K. Marek, Cheryl A. Halter, Alice Rudolph, Clifford W. Shults, Tatiana Foroud and William C. Nichols Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease Movement Disorders 21

Version of Record online: 31 OCT 2006 | DOI: 10.1002/mds.21162

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