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Volumn 115, Issue 9, 2008, Pages 1275-1277

LRRK2 Gly2385Arg mutation and clinical features in a Chinese population with early-onset Parkinson's disease compared to late-onset patients

Author keywords

Chinese; Early onset Parkinson's disease; LRRK2 Gly2385Arg mutation

Indexed keywords

ARGININE; LEUCINE RICH REPEAT KINASE 2;

EID: 50649115505     PISSN: 03009564     EISSN: 14351463     Source Type: Journal    
DOI: 10.1007/s00702-008-0065-0     Document Type: Article
Times cited : (19)

References (13)
  • 1
    • 33644822969 scopus 로고    scopus 로고
    • Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease
    • D Berg K Schweitzer P Leitner 2005 Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease Brain 128 3000 3011
    • (2005) Brain , vol.128 , pp. 3000-3011
    • Berg, D.1    Schweitzer, K.2    Leitner, P.3
  • 2
    • 38549097049 scopus 로고    scopus 로고
    • The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease
    • L Cao T Zhang Q Xiao 2007 The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease Mov Disord 22 2439 2442
    • (2007) Mov Disord , vol.22 , pp. 2439-2442
    • Cao, L.1    Zhang, T.2    Xiao, Q.3
  • 3
    • 0942300688 scopus 로고    scopus 로고
    • Comparison of environmental and genetic factors for Parkinson's disease between Chinese and Caucasians
    • DKY Chan D Cordato Bui Triet G Mellick 2004 Comparison of environmental and genetic factors for Parkinson's disease between Chinese and Caucasians Neuroepidemiology 23 13 22
    • (2004) Neuroepidemiology , vol.23 , pp. 13-22
    • Chan, D.K.Y.1    Cordato, D.2    Bui, T.3    Mellick, G.4
  • 4
    • 44749090091 scopus 로고    scopus 로고
    • PARK2 mutations and clinical features in a Chinese population with early onset Parkinson's disease
    • doi 10.1007/s00702-007-0011-6
    • Chan DKY, Mok V, Ng PW et al (2008) PARK2 mutations and clinical features in a Chinese population with early onset Parkinson's disease. J Neural Transm doi 10.1007/s00702-007-0011-6
    • (2008) J Neural Transm
    • Chan, D.K.Y.1    Mok, V.2    Ng, P.W.3
  • 5
    • 33746079596 scopus 로고    scopus 로고
    • A common missense variant in the LRRK2 gene, Gly2385Arg, associated with parkinson's diseae risk in Taiwan
    • A Di Fonzo YH Wu-Chou CS Lu 2006 A common missense variant in the LRRK2 gene, Gly2385Arg, associated with parkinson's diseae risk in Taiwan Neurogenetics 7 133 138
    • (2006) Neurogenetics , vol.7 , pp. 133-138
    • Di Fonzo, A.1    Wu-Chou, Y.H.2    Lu, C.S.3
  • 6
    • 33847226901 scopus 로고    scopus 로고
    • Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population
    • M Funayama Y Li H Tomiyama 2007 Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population NeuroReport 18 273 275
    • (2007) NeuroReport , vol.18 , pp. 273-275
    • Funayama, M.1    Li, Y.2    Tomiyama, H.3
  • 7
    • 33846587090 scopus 로고    scopus 로고
    • A common genetic factor for Parkinson's disease in ethnic Chinese population in Taiwan
    • HC Fung CM Chen J Hardy AB Singleton YR Wu 2006 A common genetic factor for Parkinson's disease in ethnic Chinese population in Taiwan BMC Neurol 6 47
    • (2006) BMC Neurol , vol.6 , pp. 47
    • Fung, H.C.1    Chen, C.M.2    Hardy, J.3    Singleton, A.B.4    Wu, Y.R.5
  • 8
    • 19944432921 scopus 로고    scopus 로고
    • A common LRRK2 mutation in idiopathic Parkinson's disease
    • 9457
    • WP Gilks PM Abou-Sleiman S Gandhi 2005 A common LRRK2 mutation in idiopathic Parkinson's disease Lancet 365 9457 415 416
    • (2005) Lancet , vol.365 , pp. 415-416
    • Gilks, W.P.1    Abou-Sleiman, P.M.2    Gandhi, S.3
  • 9
    • 27744446035 scopus 로고    scopus 로고
    • The I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease
    • NM_004562.1
    • Lu C, Simons E, Wu-Chou Y et al (2005) The I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease. Parkinsonism and related disorders 11(8):521-522. NM_004562.1 http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?val=83722281&from=121&to= 7704&view=gbwithparts
    • (2005) Parkinsonism and Related Disorders , vol.11 , Issue.8 , pp. 521-522
    • Lu, C.1    Simons, E.2    Wu-Chou, Y.3
  • 10
    • 8844266996 scopus 로고    scopus 로고
    • Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
    • 4
    • C Paisan-Ruiz S Jain EW Evans 2004 Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease Neuron 44 4 595 600
    • (2004) Neuron , vol.44 , pp. 595-600
    • Paisan-Ruiz, C.1    Jain, S.2    Evans, E.W.3
  • 11
    • 33846358949 scopus 로고    scopus 로고
    • The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: Genetic and functional evidence
    • EK Tan Y Zhao L Skipper 2007 The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence Hum Genet 120 857 863
    • (2007) Hum Genet , vol.120 , pp. 857-863
    • Tan, E.K.1    Zhao, Y.2    Skipper, L.3
  • 12
    • 32044458576 scopus 로고    scopus 로고
    • LRRK2: A common pathway for parkinsonism, pathogenesis and prevention?
    • JP Taylor IF Mata MJ Farrer 2006 LRRK2: a common pathway for parkinsonism, pathogenesis and prevention? Trends Mol Med 12 76 82
    • (2006) Trends Mol Med , vol.12 , pp. 76-82
    • Taylor, J.P.1    Mata, I.F.2    Farrer, M.J.3
  • 13
    • 8844233579 scopus 로고    scopus 로고
    • Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
    • 4
    • A Zimprich S Biskup P Leitner 2004 Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology Neuron 44 4 601 607
    • (2004) Neuron , vol.44 , pp. 601-607
    • Zimprich, A.1    Biskup, S.2    Leitner, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.