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Volumn 24, Issue 3, 2004, Pages 262-265

Exon deletions of parkin gene in patients with Parkinson disease

Author keywords

Deletive mutation; Parkin gene; Parkinson disease

Indexed keywords

DISEASES; ELECTROPHORESIS; PATHOLOGY;

EID: 27644511639     PISSN: 0257716X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (8)
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  • 2
    • 0033933048 scopus 로고    scopus 로고
    • Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase
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    • Shimura, H.1    Hattori, N.2    Kubo, S.3
  • 3
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    • Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
    • Kitada T, Asakawa S, Hattori N et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature, 1998, 392:605
    • (1998) Nature , vol.392 , pp. 605
    • Kitada, T.1    Asakawa, S.2    Hattori, N.3
  • 4
    • 0342368772 scopus 로고    scopus 로고
    • Association between early-onset Parkinson's disease and mutations in the parkin gene
    • Lücking C B, Dürr A, Bonifati V et al. Association between early-onset Parkinson's disease and mutations in the parkin gene. N Engl J Med, 2000, 342:1560
    • (2000) N Engl J Med , vol.342 , pp. 1560
    • Lücking, C.B.1    Dürr, A.2    Bonifati, V.3
  • 5
    • 0034682718 scopus 로고    scopus 로고
    • Structure of a c-cbl-UbcH7 complex; ring domain function in ubiquitin-protein ligases
    • Zheng N, Wang P, Jeffrey P D et al. Structure of a c-cbl-UbcH7 complex; ring domain function in ubiquitin-protein ligases. Cell, 2000, 102:533
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    • Zheng, N.1    Wang, P.2    Jeffrey, P.D.3
  • 6
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    • All in the ubiquitin family
    • Hochstrasser M. All in the ubiquitin family. Science, 2000, 289:563
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    • Hochstrasser, M.1
  • 7
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    • Parkin deletions in a family with adult-onset, tremor-dominant parkin-sonism; expanding the phenotype
    • Klein C, Pramstaller P P, Kis B et al. Parkin deletions in a family with adult-onset, tremor-dominant parkin-sonism; expanding the phenotype. Ann Neurol, 2000, 48:65
    • (2000) Ann Neurol , vol.48 , pp. 65
    • Klein, C.1    Pramstaller, P.P.2    Kis, B.3
  • 8
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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-Matsumine 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
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.