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Volumn 19, Issue 9, 2012, Pages

VPS35 mutation in Chinese Han patients with late-onset Parkinson's disease

Author keywords

Chinese Han; Late onset Parkinson's disease; The VPS35 gene

Indexed keywords

LEUCINE RICH REPEAT KINASE 2;

EID: 84865286979     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2012.03800.x     Document Type: Letter
Times cited : (15)

References (11)
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  • 3
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    • A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease
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  • 4
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    • Screening for VPS35 mutations in Parkinson's disease
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  • 5
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    • The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease
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    • Verstraeten, A.1    Wauters, E.2    Crosiers, D.3
  • 7
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    • Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease
    • Zhang Y, Chen S, Xiao Q, et al. Vacuolar protein sorting 35 Asp620Asn mutation is rare in the ethnic Chinese population with Parkinson's disease. Parkinsonism Relat Disord 2012; 18: 638-640.
    • (2012) Parkinsonism Relat Disord , vol.18 , pp. 638-640
    • Zhang, Y.1    Chen, S.2    Xiao, Q.3
  • 8
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    • The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
    • Rogaeva E, Meng Y, Lee JH, et al. The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease. Nat Genet 2007; 39: 168-177.
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  • 9
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    • Frameshift mutations of vacuolar protein sorting genes in gastric and colorectal cancers with microsatellite instability
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    • The LRRK2 G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers
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    • VPS35 haploinsufficiency increases Alzheimer's disease neuropathology
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.