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Volumn 54, Issue 2, 2000, Pages 504-507

A kindred with Parkinson's disease not showing genetic linkage to established loci

Author keywords

Familial PD; Linkage exclusion; Postural tremor

Indexed keywords

ALPHA SYNUCLEIN;

EID: 0034711720     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.54.2.504     Document Type: Article
Times cited : (19)

References (10)
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    • Leroy, E.1    Boyer, R.2    Auburger, G.3
  • 5
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    • A chromosome 4phaplotype segregating with Parkinson's disease and postural tremor
    • Farrer M, Gwinn-Hardy K, Muenter M, et al. A chromosome 4phaplotype segregating with Parkinson's disease and postural tremor. Hum Mol Genet 1999;8:81-85.
    • (1999) Hum Mol Genet , vol.8 , pp. 81-85
    • Farrer, M.1    Gwinn-Hardy, K.2    Muenter, M.3
  • 6
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    • Et al Mutation in the α-synuclein gene identified in families with Parkinson's disease
    • Polymeropoulos MH, Lavedan C, Leroy E, et al Mutation in the α-synuclein gene identified in families with Parkinson's disease. Science 1997;276:2045-2048.
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  • 7
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    • Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27
    • Matsumine H, Saito M, Shimoda-Matsubayashi S, et al. Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27. Am J Hum Genet 1997;60:588-596.
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  • 8
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    • Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus
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    • The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recording and fuzzy inheritance
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.