메뉴 건너뛰기




Volumn 1296, Issue , 2009, Pages 113-116

LRRK2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China

Author keywords

Case control study; LRRK2 R1628P; Parkinson's disease; Single nucleotide polymorphism

Indexed keywords

LEUCINE RICH REPEAT KINASE 2;

EID: 70349267492     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2009.08.047     Document Type: Article
Times cited : (23)

References (18)
  • 3
    • 0015154543 scopus 로고
    • Attributable risk percent in case-control studies
    • Cole P., and Macmahon B. Attributable risk percent in case-control studies. Br. J. Prev. Soc. Med. 25 (1971) 242-244
    • (1971) Br. J. Prev. Soc. Med. , vol.25 , pp. 242-244
    • Cole, P.1    Macmahon, B.2
  • 5
    • 0038727936 scopus 로고    scopus 로고
    • Description of Parkinson's disease as a clinical syndrome
    • Fahn S. Description of Parkinson's disease as a clinical syndrome. Ann. N. Y. Acad. Sci. 991 (2003) 1-14
    • (2003) Ann. N. Y. Acad. Sci. , vol.991 , pp. 1-14
    • Fahn, S.1
  • 7
    • 33745034020 scopus 로고    scopus 로고
    • Parkinson's disease: the genetics of a heterogeneous disorder
    • Gosal D., Ross O.A., and Toft M. Parkinson's disease: the genetics of a heterogeneous disorder. Eur. J. Neurol. 13 (2006) 616-627
    • (2006) Eur. J. Neurol. , vol.13 , pp. 616-627
    • Gosal, D.1    Ross, O.A.2    Toft, M.3
  • 8
    • 0026514953 scopus 로고
    • Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases
    • Hughes A.J., Daniel S.E., Kilford L., and Lees A.J. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J. Neurol. Neurosurg. Psychiatry 55 (1992) 181-184
    • (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
  • 9
    • 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
    • Lesage S., Leutenegger A.L., Ibanez P., Janin S., Lohmann E., Dürr A., and Brice A. 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. 77 (2005) 330-332
    • (2005) Am. J. Hum. Genet. , vol.77 , pp. 330-332
    • Lesage, S.1    Leutenegger, A.L.2    Ibanez, P.3    Janin, S.4    Lohmann, E.5    Dürr, A.6    Brice, A.7
  • 13
    • 19344378419 scopus 로고    scopus 로고
    • Prevalence of Parkonson's disease in China
    • Rocca W.A. Prevalence of Parkonson's disease in China. Lancet Neurol. 4 (2005) 328-329
    • (2005) Lancet Neurol. , vol.4 , pp. 328-329
    • Rocca, W.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.