메뉴 건너뛰기




Volumn 59, Issue 2, 2011, Pages 157-160

LRRK2 G2019S mutation does not contribute to Parkinson′s disease in South India

Author keywords

G2019S mutation; India; LRRK2; Parkinson s disease

Indexed keywords

DNA; LEUCINE RICH REPEAT KINASE 2;

EID: 79955432541     PISSN: 00283886     EISSN: 19984022     Source Type: Journal    
DOI: 10.4103/0028-3886.79125     Document Type: Article
Times cited : (21)

References (30)
  • 1
    • 67749118059 scopus 로고    scopus 로고
    • LRRK2 gene variation and its contribution to Parkinson disease
    • Paisan-Ruiz C. LRRK2 gene variation and its contribution to Parkinson disease. Hum Mutat 2009;30:1153-60.
    • (2009) Hum Mutat , vol.30 , pp. 1153-1160
    • Paisan-Ruiz, C.1
  • 2
    • 68949125734 scopus 로고    scopus 로고
    • Zeroing in on LRRK2-linked pathogenic mechanisms in Parkinson's disease
    • Biskup S, West AB. Zeroing in on LRRK2-linked pathogenic mechanisms in Parkinson's disease. Biochim Biophys Acta 2009;1792:625-33.
    • (2009) Biochim Biophys Acta , vol.1792 , pp. 625-633
    • Biskup, S.1    West, A.B.2
  • 3
    • 50049104725 scopus 로고    scopus 로고
    • Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: A case-control study
    • Healy DG, Falchi M, O'Sullivan SS, Bonifati V, Durr A, Bressman S, et al. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol 2008;7:583-90.
    • (2008) Lancet Neurol , vol.7 , pp. 583-590
    • Healy, D.G.1    Falchi, M.2    O'Sullivan, S.S.3    Bonifati, V.4    Durr, A.5    Bressman, S.6
  • 6
    • 33645160640 scopus 로고    scopus 로고
    • The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor
    • Goldwurm S, Di Fonzo A, Simons EJ, Rohé CF, Zini M, Canesi M, et al. The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor. J Med Genet 2005;42:e65.
    • (2005) J Med Genet , vol.42
    • Goldwurm, S.1    Di Fonzo, A.2    Simons, E.J.3    Rohé, C.F.4    Zini, M.5    Canesi, M.6
  • 7
    • 79958116682 scopus 로고    scopus 로고
    • Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries
    • Bar-Shira A, Hutter CM, Giladi N, Zabetian CP, Orr-Urtreger A. Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries. Neurogenetics 2009;10:355-8.
    • (2009) Neurogenetics , vol.10 , pp. 355-358
    • Bar-Shira, A.1    Hutter, C.M.2    Giladi, N.3    Zabetian, C.P.4    Orr-Urtreger, A.5
  • 9
    • 76549094100 scopus 로고    scopus 로고
    • Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India
    • Vinish M, Prabhakar S, Khullar M, Verma I, Anand A. Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India. J Neurol Neurosurg Psychiatry 2010;81:166-70.
    • (2010) J Neurol Neurosurg Psychiatry , vol.81 , pp. 166-170
    • Vinish, M.1    Prabhakar, S.2    Khullar, M.3    Verma, I.4    Anand, A.5
  • 11
    • 27444434729 scopus 로고    scopus 로고
    • Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease
    • DOI 10.1136/jnnp.2004.046888
    • Madegowda RH, Kishore A, Anand A. Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease. J Neurol Neurosurg Psychiatry 2005;76:1588-90. (Pubitemid 41531714)
    • (2005) Journal of Neurology, Neurosurgery and Psychiatry , vol.76 , Issue.11 , pp. 1588-1590
    • Madegowda, R.H.1    Kishore, A.2    Anand, A.3
  • 12
    • 0026514953 scopus 로고
    • Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinico-pathological study of 100 cases
    • Hughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry 1992;55:181-4.
    • (1992) J Neurol Neurosurg Psychiatry , vol.55 , pp. 181-184
    • Hughes, A.J.1    Daniel, S.E.2    Kilford, L.3    Lees, A.J.4
  • 14
    • 0033990048 scopus 로고    scopus 로고
    • Primer3 on the WWW for general users and for biologist programmers
    • Krawetz S, Misener S, editors, Totowa, New Jersey: Humana Press
    • Rozen S, Skaletsky H. Primer3 on the WWW for general users and for biologist programmers. In: Krawetz S, Misener S, editors. Bioinformatics Methods and Protocols: Methods in Molecular Biology. Totowa, New Jersey: Humana Press; 2000. p. 365-86.
    • (2000) Bioinformatics Methods and Protocols: Methods in Molecular Biology , pp. 365-386
    • Rozen, S.1    Skaletsky, H.2
  • 18
    • 67651166905 scopus 로고    scopus 로고
    • A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients
    • Shojaee S, Sina F, Farboodi N, Fazlali Z, Ghazavi F, Ghorashi SA, et al. A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients. Mov Disord 2009;24:1023-7.
    • (2009) Mov Disord , vol.24 , pp. 1023-1027
    • Shojaee, S.1    Sina, F.2    Farboodi, N.3    Fazlali, Z.4    Ghazavi, F.5    Ghorashi, S.A.6
  • 19
    • 22544465257 scopus 로고    scopus 로고
    • LRRK2 haplotype analyses in European and North African families with Parkinson disease: A common founder for the G2019S mutation dating from the 13th century [2]
    • DOI 10.1086/432422
    • Lesage S, Leutenegger AL, Ibanez P, Janin S, Lohmann E, Dürr A, et al. LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century. Am J Hum Genet 2005;77:330-2. (Pubitemid 41022715)
    • (2005) American Journal of Human Genetics , vol.77 , Issue.2 , pp. 330-332
    • Lesage, S.1    Leutenegger, A.-L.2    Ibanez, P.3    Janin, S.4    Lohmann, E.5    Durr, A.6    Brice, A.7
  • 20
    • 38349189767 scopus 로고    scopus 로고
    • A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease
    • Warren L, Gibson R, Ishihara L, Elango R, Xue Z, Akkari A, et al. A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease. Parkinsonism Relat Disord 2008;14:77-80.
    • (2008) Parkinsonism Relat Disord , vol.14 , pp. 77-80
    • Warren, L.1    Gibson, R.2    Ishihara, L.3    Elango, R.4    Xue, Z.5    Akkari, A.6
  • 23
    • 48849095698 scopus 로고    scopus 로고
    • The ancestry of LRRK2 Gly2019Ser Parkinsonism
    • Benamer HT. The ancestry of LRRK2 Gly2019Ser Parkinsonism. Lancet Neurol 2008;7:769-70.
    • (2008) Lancet Neurol , vol.7 , pp. 769-770
    • Benamer, H.T.1
  • 27
    • 73449090031 scopus 로고    scopus 로고
    • The G2019S LRRK2 mutation is rare in Korean patients with Parkinson's disease and multiple system atrophy
    • Cho JW, Kim SY, Park SS, Jeon BS. The G2019S LRRK2 mutation is rare in Korean patients with Parkinson's disease and multiple system atrophy. J Clin Neurol 2009;5:29-32.
    • (2009) J Clin Neurol , vol.5 , pp. 29-32
    • Cho, J.W.1    Kim, S.Y.2    Park, S.S.3    Jeon, B.S.4
  • 28
    • 52649172690 scopus 로고    scopus 로고
    • Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease
    • Choi JM, Woo MS, Ma HI, Kang SY, Sung YH, Yong SW, et al. Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease. Neurogenetics 2008;9:263-9.
    • (2008) Neurogenetics , vol.9 , pp. 263-269
    • Choi, J.M.1    Woo, M.S.2    Ma, H.I.3    Kang, S.Y.4    Sung, Y.H.5    Yong, S.W.6
  • 29
    • 33745862378 scopus 로고    scopus 로고
    • Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease
    • DOI 10.1002/mds.20814
    • Fung HC, Chen CM, Hardy J, Hernandez D, Singleton A, Wu YR. Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease. Mov Disord 2006;21:880-1. (Pubitemid 44028316)
    • (2006) Movement Disorders , vol.21 , Issue.6 , pp. 880-881
    • Fung, H.-C.1    Chen, C.-M.2    Hardy, J.3    Hernandez, D.4    Singleton, A.5    Wu, Y.-R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.