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Volumn 17, Issue 1, 1997, Pages 65-70

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CEREBELLAR ATAXIA; CHILD PARENT RELATION; CHROMOSOME 3P; CLINICAL ARTICLE; DISEASE ASSOCIATION; GENE ISOLATION; GENE LOCATION; HUMAN; ONSET AGE; PRIORITY JOURNAL; RETINA MACULA DEGENERATION;

EID: 16944364511     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0997-65     Document Type: Article
Times cited : (713)

References (14)
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    • Clinical features and classification of inherited ataxias
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    • Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy: A clinical and genetic study of eight families
    • Enevoldson, T.P., Sanders, M.D. & Harding, A.E. Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy: a clinical and genetic study of eight families. Brain 117, 445-460 (1994).
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  • 6
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    • Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I
    • Benomar, A. et al. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I. Ann. Neurol. 35, 439-444 (1994).
    • (1994) Ann. Neurol. , vol.35 , pp. 439-444
    • Benomar, A.1
  • 7
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    • The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1
    • Benomar, A. et al. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1. Nature Genet 10, 84-88 (1995).
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    • Benomar, A.1
  • 8
    • 19244364538 scopus 로고    scopus 로고
    • The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: Genetic and physical mapping of the SCA7 locus
    • David, G. et al. The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus. Am. J. Hum. Genet 59, 1328-1336 (1996).
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    • Localization of autosomal dominant cerebellar ataxia associated with retinal degeneration and anticipation to chromosome 3p12-p21.1
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.