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Volumn 42, Issue 4, 1999, Pages 217-220

Absence of G209A and G88C mutations in the alpha-synuclein gene of Parkinson's disease in a Chinese population

Author keywords

Alpha synuclein gene; Chinese; Genetic mutation; Parkinson's disease; Pathogenesis

Indexed keywords

ALPHA SYNUCLEIN;

EID: 0032697860     PISSN: 00143022     EISSN: None     Source Type: Journal    
DOI: 10.1159/000008110     Document Type: Article
Times cited : (18)

References (17)
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    • Payami, H.1    Larsen, K.2    Bernard, S.3    Nutt, J.4
  • 9
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    • Parkinson's Disease Society Brain Bank, London: Overview and research
    • Daniel SE, Lees AJ: Parkinson's Disease Society Brain Bank, London: Overview and research. J Neurol Transm Suppl 1993;39:165-172.
    • (1993) J Neurol Transm Suppl , vol.39 , pp. 165-172
    • Daniel, S.E.1    Lees, A.J.2
  • 10
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    • Parkinsonism: Onset, progression, and mortality
    • Hoehn MM, Yahr MD: Parkinsonism: Onset, progression, and mortality. Neurology 1967; 17:427-442.
    • (1967) Neurology , vol.17 , pp. 427-442
    • Hoehn, M.M.1    Yahr, M.D.2
  • 12
    • 0031900214 scopus 로고    scopus 로고
    • Absence of mutations in the coding region of the α-synuclein gene in pathologically proven Parkinson's disease
    • Chan P, Jiang X, Forno LS, Di Monte DA, Tanner CM, Langston JW: Absence of mutations in the coding region of the α-synuclein gene in pathologically proven Parkinson's disease. Neurology 1998;50:1136-1137.
    • (1998) Neurology , vol.50 , pp. 1136-1137
    • Chan, P.1    Jiang, X.2    Forno, L.S.3    Di Monte, D.A.4    Tanner, C.M.5    Langston, J.W.6
  • 13
    • 0031658510 scopus 로고    scopus 로고
    • The role of the α-synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom
    • Warner TT, Schapira AHV: The role of the α-synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom. J Neurol Neurosurg Psychiatry 1998;65: 378-379.
    • (1998) J Neurol Neurosurg Psychiatry , vol.65 , pp. 378-379
    • Warner, T.T.1    Schapira, A.H.V.2
  • 14
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    • Lack of mutation G209A in the α-synuclein gene in French patients with familial and sporadic Parkinson's disease
    • Lucotte G, Mercier G, Turpin JC: Lack of mutation G209A in the α-synuclein gene in French patients with familial and sporadic Parkinson's disease. J Neurol Neurosurg Psychiatry 1998;65:948-949.
    • (1998) J Neurol Neurosurg Psychiatry , vol.65 , pp. 948-949
    • Lucotte, G.1    Mercier, G.2    Turpin, J.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.