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patient mutation disease lrrk 2 parkinson carrier neurology 2019ser 1441c study idiopathic pd parkinsonism family symptom department university onset idiopathic substitution research lrrk 2 mutations frequency 1441h lrrk 2-associated pd disorder penetrance estimate analysis centre institute haplotype cause hospital parkinson disease population table article consortium stage medicine qsbb series kinase incidence control lrrk 2 gene series method group mutation carriers 10 years fference genetic scale london prevalence 79 years penetrance estimates www.neurology.org domain grant protein 2-associated ffected treatment clinic feature 69 years disease duration tremor pd onset di fference duration testing lrrk 2 protein ϯ sd age pathology figure r 1441h carriers health progression
3 Most Recent Publications
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Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism
(Article)
Ross, O.A. Spanaki, C. Bonifati, V. Wu, R.M. Zabetian, C.P. Farrer, M.J. Griffith, A. Lin, C.H. Kachergus, J. Haugarvoll, K. Latsoudis, H. Plaitakis, A. Ferreira, J.J. Sampaio, C. |
2009-07-01
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Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
(Article)
Healy, D.G. Falchi, M. Ferreira, J.J. Tolosa, E. Kay, D.M. Klein, C. Williams, D.R. Marras, C. Lang, A.E. Wszolek, Z.K. Berciano, J. Schapira, A.H. O'Sullivan, S.S. Lynch, T. Bhatia, K.P. Gasser, T. Lees, A.J. Wood, N.W. Bonifati, V. Durr, A. Bressman, S. Brice, A. Aasly, J. Zabetian, C.P. Goldwurm, S. |
2008-07-01
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Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
(Article)
Haugarvoll, K. Rademakers, R. Guidi, M. Riboldazzi, G. Brown, L. Walter, U. Benecke, R. Berg, D. Gasser, T. Theuns, J. Pals, P. Cras, P. Kachergus, J. Deyn, P.P. de Engelborghs, S. Pickut, B. Uitti, R.J. Foroud, T. Nichols, W.C. Hagenah, J. Klein, C. Samii, A. Zabetian, C.P. Nuytemans, K. Bonifati, V. Broeckhoven, C. van Farrer, M.J. Wszolek, Z.K. Ross, O.A. Gibson, J.M. Tan, E.K. Gaig, C. Tolosa, E. Goldwurm, S. |
2008-04-01
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