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Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology
Author(s): Zimprich A, Biskup S, Leitner P, Lichtner P, Farrer M, Lincoln S, Kachergus J, Hulihan M, Uitti RJ, Calne DB, Stoessl AJ, Pfeiffer RF, Patenge N, Carbajal IC, Vieregge P, Asmus F, Muller-Myhsok B, Dickson DW, Meitinger T, Strom TM, Wszolek ZK, Gasser T
Source: NEURON    Volume: 44    Issue: 4    Pages: 601-607    Published: NOV 18 2004  
Times Cited: 559     References: 31     
Abstract: We have previously linked families with autosomal-dominant, late-onset parkinsonism to chromosome 12p11.2-q13.1 (PARK8). By high-resolution recombination mapping and candidate gene sequencing in 46 families, we have found six disease-segregating mutations (five missense and one putative splice site mutation) in a gene encoding a large, multifunctional protein, LRRK2 (leucine-rich repeat kinase 2). It belongs to the ROCO protein family and includes a protein kinase domain of the MAPKKK class and several other major functional domains. Within affected carriers of families A and D, six post mortem diagnoses reveal brainstem dopaminergic degeneration accompanied by strikingly diverse pathologies. These include abnormalities consistent with Lewy body Parkinson's disease, diffuse Lewy body disease, nigral degeneration without distinctive histopathology, and progressive supranuclear palsy-like pathology. Clinical diagnoses of Parkinsonism with dementia or amyotrophy or both, with their associated pathologies, are also noted. Hence, LRRK2 may be central to the pathogenesis of several major neurodegenerative disorders associated with parkinsonism.
Document Type: Article
Language: English
Reprint Address: Meitinger, T (reprint author), GSF, Natl Res Ctr Environm & Hlth, Inst Human Genet, D-85764 Neuherberg, Germany
Addresses:
1. GSF, Natl Res Ctr Environm & Hlth, Inst Human Genet, D-85764 Neuherberg, Germany
2. Univ Tubingen, Hertie Inst Clin Brain Res, Dept Neurodegenerat Dis, D-72076 Tubingen, Germany
3. Med Univ Vienna, Dept Neurol, A-1090 Vienna, Austria
4. Mayo Clin, Dept Neurosci, Jacksonville, FL 32224 USA
5. Mayo Clin, Dept Neurol, Jacksonville, FL 32224 USA
6. Univ British Columbia, Pacific Parkinsons Res Ctr, Vancouver, BC V6T 2B5 Canada
7. Univ Tennessee, Hlth Sci Ctr, Dept Neurol, Memphis, TN 38103 USA
8. Klinikum Lemgo, Dept Neurol, D-32657 Lemgo, Germany
9. Max Planck Inst Psychiat, Computat Genet Grp, D-80804 Munich, Germany
10. Tech Univ Munich, Inst Human Genet, D-81675 Munich, Germany
Publisher: CELL PRESS, 1100 MASSACHUSETTS AVE, CAMBRIDGE, MA 02138 USA
Subject Category: Neurosciences
IDS Number: 874GE
ISSN: 0896-6273
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