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Volumn 21, Issue 1, 2004, Pages 83-85

Analysis and application of SCA1 and SCA3/MJD gene CAG repeats in Han population in Northeastern China

Author keywords

Presymptomatic diagnosis; Spinocerebellar ataxia type 1; Spinocerebellar ataxia type 3

Indexed keywords

DNA FRAGMENT;

EID: 1042265222     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (4)

References (8)
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  • 2
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    • Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
    • Orr HT, Chung MY, Banfi S, et al. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet, 1993, 4: 221-226.
    • (1993) Nat Genet , vol.4 , pp. 221-226
    • Orr, H.T.1    Chung, M.Y.2    Banfi, S.3
  • 3
    • 0028143527 scopus 로고
    • CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14 q32. 1
    • Kawaguchi Y, Okamoto T, Taniwaki M, et al. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14 q32. 1. Nat Genet, 1994, 8: 221-228.
    • (1994) Nat Genet , vol.8 , pp. 221-228
    • Kawaguchi, Y.1    Okamoto, T.2    Taniwaki, M.3
  • 4
    • 0028017992 scopus 로고
    • Identification and characterization of the gene causing type 1 spinocerebellar ataxia
    • Banfi S, Servadio A, Chung MY, et al. Identification and characterization of the gene causing type 1 spinocerebellar ataxia. Nat Genet, 1994, 7: 513-520.
    • (1994) Nat Genet , vol.7 , pp. 513-520
    • Banfi, S.1    Servadio, A.2    Chung, M.Y.3
  • 5
    • 17844379460 scopus 로고    scopus 로고
    • The genomic structure and expression of MJD, the Machedo-Joseph disease gene
    • Iachikawa Y, Goto J, Hattori, et al. The genomic structure and expression of MJD, the Machedo-Joseph disease gene. J Hum Genet, 2001, 46: 413-422.
    • (2001) J Hum Genet , vol.46 , pp. 413-422
    • Ichikawa, Y.1    Goto, J.2    Hattori3
  • 6
    • 0032777834 scopus 로고    scopus 로고
    • Spinocerebellar ataxias in Spanish patients: Genetic analysis of familial and sporadic cases
    • Pujana MA, Corral J, Gratacos M, et al. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. Hum Genet, 1999, 104: 516-522.
    • (1999) Hum Genet , vol.104 , pp. 516-522
    • Pujana, M.A.1    Corral, J.2    Gratacos, M.3
  • 7
    • 0033934458 scopus 로고    scopus 로고
    • Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2, and SCA6 loci in nine ethnic populations of eastern India
    • Basu P, Chattopadhyay B, Gangopadhaya PK, et al. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2, and SCA6 loci in nine ethnic populations of eastern India. Hum Genet, 2000, 106: 597-604.
    • (2000) Hum Genet , vol.106 , pp. 597-604
    • Basu, P.1    Chattopadhyay, B.2    Gangopadhaya, P.K.3
  • 8
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    • CAG trinacleotide mutation in patients with hereditary spinocerebellar ataxia
    • Tang BS, Xia JH, Wang DA, et al. CAG trinacleotide mutation in patients with hereditary spinocerebellar ataxia. Chin J Med Genet, 1999, 16: 281-284.
    • (1999) Chin J Med Genet , vol.16 , pp. 281-284
    • Tang, B.S.1    Xia, J.H.2    Wang, D.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.