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Volumn 51, Issue 3, 1998, Pages 887-889

Lewy body in neurodegeneration with brain iron accumulation type 1 is immunoreactive for α-synuclein

Author keywords

[No Author keywords available]

Indexed keywords

IRON;

EID: 0031721278     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.51.3.887     Document Type: Article
Times cited : (163)

References (10)
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    • Polymeropoulos MH, Lavedan C, Leroy E, et al. Mutation in the α-synuclein gene identified in families with Parkinson's disease. Science 1997;276:2045-2047.
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    • Homozygosity mapping of Hallervoprden-Spatz syndrome to chromosome 20p12.3-p13
    • Taylor TD, Litt M, Kramer P, et al. Homozygosity mapping of Hallervoprden-Spatz syndrome to chromosome 20p12.3-p13. Nature Genet 1996;14:479-481.
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    • Taylor, T.D.1    Litt, M.2    Kramer, P.3
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    • Molecular cloning of cDNA encoding an unrecognized component of amyloid in Alzheimer disease
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    • Ala30Pro mutation in the gene encoding α-synuclein in Parkinson's disease
    • Kruger R, Kuhn W, Mller T, et al. Ala30Pro mutation in the gene encoding α-synuclein in Parkinson's disease. Nature Genet 1998;18:106-108.
    • (1998) Nature Genet , vol.18 , pp. 106-108
    • Kruger, R.1    Kuhn, W.2    Mller, T.3
  • 9
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    • Identification of Spanish familial Parkinson's disease and screening for the Ala53Thr mutation of the α-synuclein gene in early onset patients
    • Munoz E, Oliva R, Obach V, et al. Identification of Spanish familial Parkinson's disease and screening for the Ala53Thr mutation of the α-synuclein gene in early onset patients. Neurosci Lett 1997;235:57-60.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.