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Volumn 61, Issue 2, 2004, Pages 183-184

Spinocerebellar Ataxia Type 17: Latest Member of Polyglutamine Disease Group Highlights Unanswered Questions

Author keywords

[No Author keywords available]

Indexed keywords

POLYGLUTAMIC ACID; TATA BINDING PROTEIN; TRINUCLEOTIDE;

EID: 1042302765     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.61.2.183     Document Type: Editorial
Times cited : (4)

References (11)
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    • Koide R, Kobayashi S, Shimohata T, et al. A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease? Hum Mol Genet. 1999;8:2047-2053.
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    • Koide, R.1    Kobayashi, S.2    Shimohata, T.3
  • 2
    • 0035393427 scopus 로고    scopus 로고
    • SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein
    • Nakamura K, Jeong SY, Uchihara T, et al. SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein. Hum Mol Genet. 2001;10:1441-1448.
    • (2001) Hum Mol Genet , vol.10 , pp. 1441-1448
    • Nakamura, K.1    Jeong, S.Y.2    Uchihara, T.3
  • 3
    • 0035076389 scopus 로고    scopus 로고
    • Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia
    • Zuhlke C, Hellenbroich Y, Dalski A, et al. Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia. Eur J Hum Genet. 2001;9:160-164.
    • (2001) Eur J Hum Genet , vol.9 , pp. 160-164
    • Zuhlke, C.1    Hellenbroich, Y.2    Dalski, A.3
  • 4
    • 0037819516 scopus 로고    scopus 로고
    • Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes
    • Stevanin G, Fujigasaki H, Lebre AS, et al. Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes. Brain 2003; 126(pt 7):1599-1603.
    • (2003) Brain , vol.126 , Issue.PART 7 , pp. 1599-1603
    • Stevanin, G.1    Fujigasaki, H.2    Lebre, A.S.3
  • 6
    • 0037321835 scopus 로고    scopus 로고
    • Phenotypical variability of expanded alleles in the TATA-binding protein gene: Reduced penetrance in SCA17?
    • Zuhlke C, Gehlken U, Hellenbroich Y, Schwinger E, Burk K. Phenotypical variability of expanded alleles in the TATA-binding protein gene: reduced penetrance in SCA17? J Neurol. 2003;250:161-163.
    • (2003) J Neurol , vol.250 , pp. 161-163
    • Zuhlke, C.1    Gehlken, U.2    Hellenbroich, Y.3    Schwinger, E.4    Burk, K.5
  • 7
    • 10744232450 scopus 로고    scopus 로고
    • Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17
    • Oda M, Maruyami H, Komure O, et al. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17. Arch Neurol. 2004;61:209-212.
    • (2004) Arch Neurol , vol.61 , pp. 209-212
    • Oda, M.1    Maruyami, H.2    Komure, O.3
  • 8
    • 0029431673 scopus 로고
    • Does homozygosity advance the onset of dentatorubral-pallidoluysian atrophy?
    • Sato K, Kashihara K, Okada S, et al. Does homozygosity advance the onset of dentatorubral-pallidoluysian atrophy? Neurology. 1995;45:1934-1936.
    • (1995) Neurology , vol.45 , pp. 1934-1936
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  • 9
    • 0029009456 scopus 로고
    • Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease
    • Takiyama Y, Igarashi S, Rogaeva EA et al. Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease. Hum Mol Genet. 1995;4:1137-1146.
    • (1995) Hum Mol Genet , vol.4 , pp. 1137-1146
    • Takiyama, Y.1    Igarashi, S.2    Rogaeva, E.A.3
  • 10
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    • Sisters homozygous for the spinocerebellar ataxia type 6(SCA6)/CACNA1A gene associated with different clinical phenotypes
    • Kato T, Tanaka F, Yamamoto M, et al. Sisters homozygous for the spinocerebellar ataxia type 6(SCA6)/CACNA1A gene associated with different clinical phenotypes. Clin Genet 2000;58:69-73.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.