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Dive into the research topics of 'Mutations in LRRK2 other than G2019S are rare in a north-American based sample of familial Parkinson's didease'. Together they form a unique fingerprint.- Sort by
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Nathan Pankratz, Michael W. Pauciulo, Veronika E. Elsaesser, Diane K. Marek, Cheyl A. Halter, Alice Rudolph, Clifford W. Shults, Tatiana Foroud, William C. Nichols, C. Shults, F. Marshall, D. Oakes, A. Shinaman, K. Marder, P. M. Conneally, K. Lyons, E. Siemers, S. Factor, D. Higgins, S. Evans
Research output: Contribution to journal › Article › peer-review