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American Journal of Human Genetics
Volumn 59, Issue 6, 1996, Pages 1328-1336
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
Author keywords

[No Author keywords available]
Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CEREBELLAR ATAXIA; CHILD; CHROMOSOME 3P; CLINICAL ARTICLE; FAMILY STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENE MAPPING; HAPLOTYPE; HUMAN; INFANT; ONSET AGE; PRIORITY JOURNAL; SYMPTOMATOLOGY;
EID: 19244364538     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (64)
References (9)
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    • Benomar A, Krols L, Stevanin G, Cancel G, Le Guern E, David G, Ouhabi H, et al (1995) The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3pl2-p21.1. Nat Genet 10:84-88
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    • Benomar, A.1    Krols, L.2    Stevanin, G.3    Cancel, G.4    Le Guern, E.5    David, G.6    Ouhabi, H.7
  • 3
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    • Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I
    • Benomar A, Le Guern E, Dürr A, Ouhabi H, Stevanin G, Yahyaoui M, Chkili T, et al (1994) Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I. Ann Neurol 35:439-444
    • (1994) Ann Neurol , vol.35 , pp. 439-444
    • Benomar, A.1    Le Guern, E.2    Dürr, A.3    Ouhabi, H.4    Stevanin, G.5    Yahyaoui, M.6    Chkili, T.7
  • 4
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    • Prevention of pre-PCR mis-priming and primer dimerization improves low-copy-number amplifications
    • Chou Q, Rüssel M, Birch DE, Raymond J, Bloch W (1992) Prevention of pre-PCR mis-priming and primer dimerization improves low-copy-number amplifications. Nucleic Acids Res 20:1717-1723
    • (1992) Nucleic Acids Res , vol.20 , pp. 1717-1723
    • Chou, Q.1    Rüssel, M.2    Birch, D.E.3    Raymond, J.4    Bloch, W.5
  • 6
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    • A comprehensive genetic map of the human genome based on 5,264 microsatellites
    • Dib C, Fauré S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, et al (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154
    • (1996) Nature , vol.380 , pp. 152-154
    • Dib, C.1    Fauré, S.2    Fizames, C.3    Samson, D.4    Drouot, N.5    Vignal, A.6    Millasseau, P.7
  • 7
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    • Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity
    • Dürr A, Chneiweiss H, Khati C, Stevanin G, Cancel G, Feingold J, Agid Y, et al (1993) Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity. Brain 116:1497-1508
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    • Dürr, A.1    Chneiweiss, H.2    Khati, C.3    Stevanin, G.4    Cancel, G.5    Feingold, J.6    Agid, Y.7
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    • Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy: A clinical and genetic study of eight families
    • Enevoldson TP, Sanders MD, Harding AE (1994) Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy: a clinical and genetic study of eight families. Brain 117:445-460
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    • Enevoldson, T.P.1    Sanders, M.D.2    Harding, A.E.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.