DCTN1 mutations in Perry syndrome (original) (raw)
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Acknowledgements
We are grateful to all family members who participated in the study. We thank L. Thal posthumously for his clinical contribution. We also thank J. Aasly, F. Hentati, T. Lynch, Y. Mizuno, R. Uitti and R.-M. Wu for their contribution and continued collaboration. S. Cobb, C. Kent and S. Lincoln provided technical support, whereas S. Hawley, F. Pishotta and C. Younkin helped with computing and bioinformatics. A.J.S., M.J.F. and Z.K.W. are funded by the Pacific Alzheimer Research Foundation (PARF) grant C06-01. Mayo Clinic Jacksonville is a Morris K. Udall Parkinson's Disease Research Center of Excellence (NINDS P50 NS40256).
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Author notes
- Mary M Hulihan and Jennifer M Kachergus: These authors contributed equally to this work.
Authors and Affiliations
- Division of Neurogenetics, Department of Neuroscience, Mayo Clinic Florida, Jacksonville, 32224, Florida, USA
Matthew J Farrer, Mary M Hulihan, Jennifer M Kachergus, Justus C Dächsel, Christian Wider, Carles Vilariño-Güell & Owen A Ross - Department of Neurology, Pacific Parkinson's Research Centre, Vancouver, VT6 2B5 BC, Canada
A Jon Stoessl, Linda L Grantier, Susan Calne & Donald B Calne - Neurology Service and Laboratory of Pathology, CHU-Caen, Caen, 14000, France
Bernard Lechevalier & Francoise Chapon - Department of Neurology, Fukuoka University, Fukuoka, 8140180, Japan
Yoshio Tsuboi & Tatsuo Yamada - Department of Neurology, West Virginia University, Morgantown, West Virginia, 26506, USA
Ludwig Gutmann - Department of Neurology, Hacettepe University School of Medicine, Ankara, 06100, Turkey
Bülent Elibol - Department of Neurology, Queen Square, University College London, London, WC1N 3BG, UK
Kailash P Bhatia - Department of Neurology, Mayo Clinic Florida, Jacksonville, Florida, 32224, USA
Christian Wider, Laura A Brown & Zbigniew K Wszolek - Department of Neuropathology, Mayo Clinic Florida, Jacksonville, Florida, 32224, USA
Monica Castanedes-Casey & Dennis W Dickson
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- Matthew J Farrer
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Contributions
M.J.F. designed and directed the genetic study and wrote and edited the manuscript. M.M.H. and J.M.K. performed the STR and linkage analysis. J.C.D. performed the protein biochemistry and cell biology. Z.K.W. directed the international clinical consortium, assisted by L.L.G., S.C., C.W. and L.A.B. A.J.S., D.B.C., B.L., F.C., Y.T., T.Y., L.G., B.E., K.P.B. and Z.K.W. performed clinical and neurologic exams. C.V.-G. and O.A.R. performed sequence and nucleotide analysis. M.C.-C. and D.W.D. performed the neuropathology and immunohistochemistry. All authors contributed to manuscript revision.
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Correspondence toMatthew J Farrer.
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Farrer, M., Hulihan, M., Kachergus, J. et al. DCTN1 mutations in Perry syndrome.Nat Genet 41, 163–165 (2009). https://doi.org/10.1038/ng.293
- Received: 24 July 2008
- Accepted: 28 October 2008
- Published: 11 January 2009
- Issue Date: February 2009
- DOI: https://doi.org/10.1038/ng.293