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Volumn 21, Issue 12, 2005, Pages 1015-1017

LRRK2: A gene belonging to the ROCO family is implicated in the Parkinson's disease;LRRK2, un gène de la famille ROCO impliquée dans la maladie de Parkinson

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; LEUCINE RICH REPEAT KINASE 2; MITOGEN ACTIVATED PROTEIN KINASE KINASE KINASE; PHOSPHOTRANSFERASE; RAS PROTEIN; UNCLASSIFIED DRUG;

EID: 30344477641     PISSN: 07670974     EISSN: None     Source Type: Journal    
DOI: 10.1051/medsci/200521121015     Document Type: Note
Times cited : (2)

References (10)
  • 1
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    • A new locus for Parkinson's disease (PARKS) maps to chromosome 12311.2-q13.1
    • Funayama M, Hasegawa K, Kowa H, et al. A new locus for Parkinson's disease (PARKS) maps to chromosome 12311.2-q13.1. Ann Neurol 2002; 51: 296-301.
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    • Funayama, M.1    Hasegawa, K.2    Kowa, H.3
  • 2
    • 8844266996 scopus 로고    scopus 로고
    • Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
    • Paisan-Ruiz C, Jain S, Evans EW, et al. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 2004; 44: 595-600.
    • (2004) Neuron , vol.44 , pp. 595-600
    • Paisan-Ruiz, C.1    Jain, S.2    Evans, E.W.3
  • 3
    • 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: 601-7.
    • (2004) Neuron , vol.44 , pp. 601-607
    • Zimprich, A.1    Biskup, S.2    Leitner, P.3
  • 4
    • 19944432606 scopus 로고    scopus 로고
    • Genetic screening for a single common LRRK2 mutation in familial Parkinson disease
    • Nichols WC, Pankratz N, Hernandez O, et al. Genetic screening for a single common LRRK2 mutation in familial Parkinson disease. Lancet 2005; 365: 410-2.
    • (2005) Lancet , vol.365 , pp. 410-412
    • Nichols, W.C.1    Pankratz, N.2    Hernandez, O.3
  • 5
    • 19944431081 scopus 로고    scopus 로고
    • A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
    • Di Fonzo A, Rohé CF, Ferreira J, et al. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. Lancet 2005; 365: 412-5.
    • (2005) Lancet , vol.365 , pp. 412-415
    • Di Fonzo, A.1    Rohé, C.F.2    Ferreira, J.3
  • 6
    • 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: 672-80.
    • (2005) Am J Hum Genet , vol.76 , pp. 672-680
    • Kachergus, J.1    Mata, I.F.2    Hulihan, M.3
  • 7
    • 27644455523 scopus 로고    scopus 로고
    • The G2019S LRRK2 mutation in French and North African families with Parkinson's disease
    • Lesage S, Ibanez P, Lohmann E, et al. The G2019S LRRK2 mutation in French and North African families with Parkinson's disease. Ann Neurol 2005 (sous presse)
    • (2005) Ann Neurol
    • Lesage, S.1    Ibanez, P.2    Lohmann, E.3
  • 8
    • 20644455323 scopus 로고    scopus 로고
    • The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients
    • Tan EK, Shen H, Tan LC, et al. The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients. Neurosci Lett 2005; 384: 327-9.
    • (2005) Neurosci Lett , vol.384 , pp. 327-329
    • Tan, E.K.1    Shen, H.2    Tan, L.C.3
  • 9
    • 19944432921 scopus 로고    scopus 로고
    • A common LRRK2 mutation in idiopathic Parkinson's disease
    • Gilks WP, Abou-Sleiman P, Gandhi S, et al. A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet 2005; 365: 415-6.
    • (2005) Lancet , vol.365 , pp. 415-416
    • Gilks, W.P.1    Abou-Sleiman, P.2    Gandhi, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.