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Volumn 101, Issue 1, 1997, Pages 18-21

Polymorphisms at 13 expressed human sequences containing CAG/CTG repeats and analysis in autosomal dominant cerebellar ataxia (ADCA) patients

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 0031469302     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050578     Document Type: Article
Times cited : (3)

References (26)
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  • 7
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    • Harding AE (1993) Clinical features and classification of inherited ataxias. In: Harding AE, Deufel P (eds) Advances in neurology, vol 61: inherited ataxias. Raven Press, pp 1-14
    • (1993) Advances in Neurology, Vol 61: Inherited Ataxias , vol.61 , pp. 1-14
    • Harding, A.E.1
  • 8
    • 0028291079 scopus 로고
    • The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27
    • Imbert G, Trottier Y, Beckmaun J, Mandel JL (1994) The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27. Genomics 21 : 667-668
    • (1994) Genomics , vol.21 , pp. 667-668
    • Imbert, G.1    Trottier, Y.2    Beckmaun, J.3    Mandel, J.L.4
  • 12
    • 0027297703 scopus 로고
    • Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms
    • Li S-H, McInnis M, Margolis R, Antonarakis S, Ross C (1993) Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms. Genomics 16 : 572-579
    • (1993) Genomics , vol.16 , pp. 572-579
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  • 15
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    • The repeat expansion detection (RED) method in the analysis of diseases with CAG/CTG repeat expansion: Usefulness and limitations
    • in press
    • Martorell L, Pujana MA, Volpini V, Sánchez A, Joven J, Vilella E, Estivill X (1997) The repeat expansion detection (RED) method in the analysis of diseases with CAG/CTG repeat expansion: usefulness and limitations. Hum Mutat (in press)
    • (1997) Hum Mutat
    • Martorell, L.1    Pujana, M.A.2    Volpini, V.3    Sánchez, A.4    Joven, J.5    Vilella, E.6    Estivill, X.7
  • 20
    • 0028020605 scopus 로고
    • Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 10
    • Ranum LPW, Schut LJ, Lundgren JK, Orr TH, Livingston DM (1995) Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 10. Nat Genet 8 : 280-284
    • (1995) Nat Genet , vol.8 , pp. 280-284
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    • Twells R, Xu W, Ball D, Allotey R, Williamson R, Chamberlain S (1995) Exclusion of the neuronal nitric oxide synthase gene and the human achete-acute homologue I gene as candidate loci for spinal cerebellar ataxia 2. Am J Hum Genet 56 : 336-337
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.