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Volumn 65, Issue 5, 2005, Pages 741-744

A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations

Author keywords

[No Author keywords available]

Indexed keywords

LEUCINE RICH REPEAT KINASE 2; PHOSPHOTRANSFERASE; UNCLASSIFIED DRUG;

EID: 24644486896     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000172630.22804.73     Document Type: Article
Times cited : (146)

References (10)
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    • Paisan-Ruiz C, Jain S, Evans EW, et al. Cloning of the gene containing mutations that cause PARKS-linked Parkinson's disease. Neuron 2004; 44:595-600.
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    • Paisan-Ruiz, C.1    Jain, S.2    Evans, E.W.3
  • 2
    • 8844233579 scopus 로고    scopus 로고
    • Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
    • Zimprich A, Biskup S, Leitner P, et al. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron 2004;44:601-607.
    • (2004) Neuron , vol.44 , pp. 601-607
    • Zimprich, A.1    Biskup, S.2    Leitner, P.3
  • 3
    • 3843066722 scopus 로고    scopus 로고
    • Unraveling the pathogenesis of Parkinson's disease-the contribution of monogenic forms
    • Bonifati V, Oostra BA, Heutink P. Unraveling the pathogenesis of Parkinson's disease-the contribution of monogenic forms. Cell Mol Life Sci 2004;61:1729-1750.
    • (2004) Cell Mol Life Sci , vol.61 , pp. 1729-1750
    • Bonifati, V.1    Oostra, B.A.2    Heutink, P.3
  • 4
    • 20144387207 scopus 로고    scopus 로고
    • Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: Evidence of a common founder across European populations
    • Kachergus J, Mata IF, Hulihan M, et al. Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations. Am J Hum Genet 2005;76:672-680.
    • (2005) Am J Hum Genet , vol.76 , pp. 672-680
    • Kachergus, J.1    Mata, I.F.2    Hulihan, M.3
  • 5
    • 19944431081 scopus 로고    scopus 로고
    • A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
    • Di Fonzo A, Rohe CF, Ferreira J, et al. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. Lancet 2005;365:412-415.
    • (2005) Lancet , vol.365 , pp. 412-415
    • Di Fonzo, A.1    Rohe, C.F.2    Ferreira, J.3
  • 6
    • 19944432606 scopus 로고    scopus 로고
    • Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
    • Nichols WC, Pankratz N, Hernandez D, et al. Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. Lancet 2005;365:410-412.
    • (2005) Lancet , vol.365 , pp. 410-412
    • Nichols, W.C.1    Pankratz, N.2    Hernandez, D.3
  • 7
    • 19944432921 scopus 로고    scopus 로고
    • A common LRRK2 mutation in idiopathic Parkinson's disease
    • Gilks WP, Abou-Sleiman PM, Gandhi S, et al. A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet 2005;365:415-416.
    • (2005) Lancet , vol.365 , pp. 415-416
    • Gilks, W.P.1    Abou-Sleiman, P.M.2    Gandhi, S.3
  • 8
    • 0026695663 scopus 로고
    • Criteria for diagnosing Parkinson's disease
    • Calne DB, Snow BJ, Lee C. Criteria for diagnosing Parkinson's disease. Ann Neurol 1992;32(suppl):S125-S127.
    • (1992) Ann Neurol , vol.32 , Issue.SUPPL.
    • Calne, D.B.1    Snow, B.J.2    Lee, C.3
  • 10
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    • How much does dardarin contribute to Parkinson's disease?
    • Brice A. How much does dardarin contribute to Parkinson's disease? Lancet 2005;365:363-364.
    • (2005) Lancet , vol.365 , pp. 363-364
    • Brice, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.