VPS35mutation in Japanese patients with typical Parkinson's disease
Published 2012 View Full Article
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Title
VPS35mutation in Japanese patients with typical Parkinson's disease
Authors
Keywords
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Journal
MOVEMENT DISORDERS
Volume 27, Issue 11, Pages 1413-1417
Publisher
Wiley
Online
2012-09-19
DOI
10.1002/mds.25145
References
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Related references
Note: Only part of the references are listed.- The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease
- (2012) Ilaria Guella et al. MOVEMENT DISORDERS
- Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population
- (2012) Aline Verstraeten et al. NEUROBIOLOGY OF AGING
- Identification of VPS35 mutations replicated in French families with Parkinson disease
- (2012) S. Lesage et al. NEUROLOGY
- Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease
- (2012) Yu Zhang et al. PARKINSONISM & RELATED DISORDERS
- A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease
- (2011) Alexander Zimprich et al. AMERICAN JOURNAL OF HUMAN GENETICS
- VPS35 Mutations in Parkinson Disease
- (2011) Carles Vilariño-Güell et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease
- (2011) Naomi Seki et al. JOURNAL OF HUMAN GENETICS
- LRRK2 signaling pathways: the key to unlocking neurodegeneration?
- (2011) Daniel C. Berwick et al. TRENDS IN CELL BIOLOGY
- Rapid screening of ATP13A2 variant with high-resolution melting analysis
- (2010) Manabu Funayama et al. MOVEMENT DISORDERS
- Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism
- (2010) H. Yoshino et al. NEUROLOGY
- α-Synuclein Gene Rearrangements in Dominantly Inherited Parkinsonism
- (2009) Pablo Ibáñez ARCHIVES OF NEUROLOGY
- Parkinson's disease: from monogenic forms to genetic susceptibility factors
- (2009) S. Lesage et al. HUMAN MOLECULAR GENETICS
- Mutation analysis for DJ-1 in sporadic and familial parkinsonism: Screening strategy in parkinsonism
- (2009) Hiroyuki Tomiyama et al. NEUROSCIENCE LETTERS
- Mutation Analysis of the PINK1 Gene in 391 Patients With Parkinson Disease
- (2008) Ryuya Kumazawa et al. ARCHIVES OF NEUROLOGY
- Retromer
- (2008) Juan S Bonifacino et al. CURRENT OPINION IN CELL BIOLOGY
- Altered vesicular dopamine storage in Parkinson's disease: a premature demise
- (2008) W. Michael Caudle et al. TRENDS IN NEUROSCIENCES
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