相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease
Ilaria Guella et al.
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Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population
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Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease
Yu Zhang et al.
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A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease
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AMERICAN JOURNAL OF HUMAN GENETICS (2011)
VPS35 Mutations in Parkinson Disease
Carles Vilarino-Gueell et al.
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Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease
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LRRK2 signaling pathways: the key to unlocking neurodegeneration?
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alpha-Synuclein Gene Rearrangements in Dominantly Inherited Parkinsonism Frequency, Phenotype, and Mechanisms
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Parkinson's disease: from monogenic forms to genetic susceptibility factors
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Mutation analysis for DJ-1 in sporadic and familial parkinsonism: Screening strategy in parkinsonism
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NEUROSCIENCE LETTERS (2009)
Mutation analysis of the PINK1 gene in 391 patients with Parkinson disease
Ryuya Kumazawa et al.
ARCHIVES OF NEUROLOGY (2008)
Altered vesicular dopamine storage in Parkinson's disease: a premature demise
W. Michael Caudle et al.
TRENDS IN NEUROSCIENCES (2008)
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries
Hiroyuki Tomiyama et al.
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Clinical heterogeneity of α-synuclein gene duplication in Parkinson's disease
K Nishioka et al.
ANNALS OF NEUROLOGY (2006)
Preserved cardiac sympathetic nerve accounts for normal cardiac uptake of MIBG in PARK2
S Orimo et al.
MOVEMENT DISORDERS (2005)
Macular microcirculation characteristics in Parkinson's disease evaluated by OCT-Angiography: a literature review
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