Funding agencies: This project was supported by R01 NS37167, R01 NS036711, the Robert P. & Judith N. Goldberg Foundation, the Bumpus Foundation, and the Harvard NeuroDiscovery Center. A portion of this research was conducted using the Linux Cluster for Genetic Analysis (LinGA-II) funded by the Robert Dawson Evans Endowment of the Department of Medicine at Boston University School of Medicine, and Boston Medical Center. Genotyping services were provided by the Center for Inherited Disease Research (CIDR), fully funded through a federal contract from the National Institutes of Health to Johns Hopkins University (contract HHSN268200782096C).
Version of Record online: 9 JUN 2011
Copyright © 2011 Movement Disorder Society
Volume 26, Issue 11, pages 2039–2044, September 2011
How to Cite
Latourelle, J. C., Hendricks, A. E., Pankratz, N., Wilk, J. B., Halter, C., Nichols, W. C., Gusella, J. F., Destefano, A. L., Myers, R. H., Foroud, T. and and the PSG–Progeni GenePD Investigators, Coordinators, and Molecular Genetic Laboratories (2011), Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease. Mov. Disord., 26: 2039–2044. doi: 10.1002/mds.23781
Relevant conflicts of interest/financial disclosures: Nothing to report.
Full financial disclosures and author roles may be found in the online version of this article.
- Issue online: 19 SEP 2011
- Version of Record online: 9 JUN 2011
- Manuscript Accepted: 11 APR 2011
- Manuscript Revised: 8 APR 2011
- Manuscript Received: 16 FEB 2011
Additional Supporting Information may be found in the online version of this article.
|MDS_23781_sm_suppinfotab1.xls||491K||Supporting Information Table S1|
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