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Volumn 54, Issue 6, 1994, Pages 959-965

Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I

Author keywords

[No Author keywords available]

Indexed keywords

REPETITIVE DNA; TRINUCLEOTIDE;

EID: 0028229119     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (103)

References (17)
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    • Chung, M.1    Ranum, L.P.W.2    Duvick, L.A.3    Servadio, A.4    Zoghbi, H.Y.5    Orr, H.T.6
  • 2
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    • Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1
    • Gispert S, Twells R, Oroczo G, Brice A, Weber J, Heredero L, Scheufler K, et al (1993) Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1. Nature Genet 4:295-299
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  • 3
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    • Human genetic diseases due to codon reiteration: Relationship to an evolutionary mechanism
    • Green H (1993) Human genetic diseases due to codon reiteration: relationship to an evolutionary mechanism. Cell 74:955-956
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    • Green, H.1
  • 4
    • 0019789150 scopus 로고
    • Genetic aspects of autosomal dominant late onset cerebellar ataxia
    • Harding AE (1981) Genetic aspects of autosomal dominant late onset cerebellar ataxia. J Med Genet 18:436-441
    • (1981) J Med Genet , vol.18 , pp. 436-441
    • Harding, A.E.1
  • 5
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    • The clinical features and classification of the late onset autosomal dominant cerebellar ataxias
    • _ (1982) The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. Brain 105:1-28
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    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
    • Huntington's Disease Collaborative Research Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72:971-983
    • (1993) Cell , vol.72 , pp. 971-983
  • 7
    • 0027257734 scopus 로고
    • The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci
    • Jodice C, Frontali M, Persichetti F, Novelletto A, Pandolfo M, Spadaro M, Giunti P, et al (1993) The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci. Hum Mol Genet 2:1383-1387
    • (1993) Hum Mol Genet , vol.2 , pp. 1383-1387
    • Jodice, C.1    Frontali, M.2    Persichetti, F.3    Novelletto, A.4    Pandolfo, M.5    Spadaro, M.6    Giunti, P.7
  • 8
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    • The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus
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    • (1993) Am J Hum Genet , vol.53 , pp. 391-400
    • Kwiatkowski Jr., T.J.1    Orr, H.T.2    Banfi, S.3    McCall, A.E.4    Jodice, C.5    Persichetti, F.6    Novelletto, A.7
  • 11
    • 0039001059 scopus 로고
    • Improved double-stranded DNA sequencing using the linear polymerase chain reaction
    • Murray V (1989) Improved double-stranded DNA sequencing using the linear polymerase chain reaction. Nucleic Acids Res 17:8889
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  • 13
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    • Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p
    • Ranum PWL, Duvick LA, Rich SS, Schut LJ, Litt M, Orr HT (1991) Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p. Am J Hum Genet 49:31-41
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  • 17
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    • The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.