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Volumn 62, Issue 4, 2004, Pages 648-651

Japanese SCA families with an unusual phenotype linked to a locus overlapping with SCA15 locus

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; ARTICLE; CHROMOSOME 3P; FEMALE; GENE; GENE LOCUS; GENE MAPPING; GENETIC ASSOCIATION; GENETIC LINKAGE; GENOME; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SCA15 GENE; SCORING SYSTEM; SPINOCEREBELLAR DEGENERATION; TREMOR;

EID: 10744232588     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000110190.08412.25     Document Type: Article
Times cited : (39)

References (10)
  • 1
    • 0035852807 scopus 로고    scopus 로고
    • Autosomal dominant spinocerebellar ataxias ad infinitum?
    • Subramony SH, Filla A. Autosomal dominant spinocerebellar ataxias ad infinitum? Neurology 2001;56:287-289.
    • (2001) Neurology , vol.56 , pp. 287-289
    • Subramony, S.H.1    Filla, A.2
  • 2
    • 0038048459 scopus 로고    scopus 로고
    • Spinocerebellar ataxia 15 (SCA15) maps to 3p24.2-3pter; exclusion of the ITPR1 gene, the human orthologue of an ataxia mouse mutant
    • Melanie AK, Marina LK, et al. Spinocerebellar ataxia 15 (SCA15) maps to 3p24.2-3pter; exclusion of the ITPR1 gene, the human orthologue of an ataxia mouse mutant. Neurobiol Dis 2003;13:147-157.
    • (2003) Neurobiol Dis , vol.13 , pp. 147-157
    • Melanie, A.K.1    Marina, L.K.2
  • 3
    • 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
  • 4
    • 0036820509 scopus 로고    scopus 로고
    • Identification of a novel SCA locus (SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21
    • Verbeek DS, Schelhaas JH, Ippel EF, et al. Identification of a novel SCA locus (SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21. Hum Genet 2002;111:388-393.
    • (2002) Hum Genet , vol.111 , pp. 388-393
    • Verbeek, D.S.1    Schelhaas, J.H.2    Ippel, E.F.3
  • 5
    • 0036830123 scopus 로고    scopus 로고
    • A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7q21.3-p15.1
    • Vuuillaume I, Devos D, Schraen-Maschke S, et al. A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7q21.3-p15.1. Ann Neurol 2002;52:666-670.
    • (2002) Ann Neurol , vol.52 , pp. 666-670
    • Vuuillaume, I.1    Devos, D.2    Schraen-Maschke, S.3
  • 6
    • 0037677603 scopus 로고    scopus 로고
    • A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23
    • Chung M-Y, Lu Y-C, Cheng N-C, et al. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23. Brain 2003;126:1293-1299.
    • (2003) Brain , vol.126 , pp. 1293-1299
    • Chung, M.-Y.1    Lu, Y.-C.2    Cheng, N.-C.3
  • 7
    • 1342311033 scopus 로고    scopus 로고
    • A new syndrome of hereditary sensory and cerebellar ataxia with muscle atrophy, SCA18: Linkage to chromosome 7q31-7q32
    • Brkanac Z, Fernandez M, Matsushita M, et al. A new syndrome of hereditary sensory and cerebellar ataxia with muscle atrophy, SCA18: linkage to chromosome 7q31-7q32. Am J Hum Genet 2001;69(suppl): 497.
    • (2001) Am J Hum Genet , vol.69 , Issue.SUPPL. , pp. 497
    • Brkanac, Z.1    Fernandez, M.2    Matsushita, M.3
  • 8
    • 0032231668 scopus 로고    scopus 로고
    • Close association between prevalences of dominantly inherited SCAs with CAG repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations
    • Takano H, Cancel G, Ikeuchi T, et al. Close association between prevalences of dominantly inherited SCAs with CAG repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations. Am J Hum Genet 1998;63:1060-1066.
    • (1998) Am J Hum Genet , vol.63 , pp. 1060-1066
    • Takano, H.1    Cancel, G.2    Ikeuchi, T.3
  • 9
    • 0034098774 scopus 로고    scopus 로고
    • Allegro, a new computer program for multipoint linkage analysis
    • Gudbjartsson DF, Jonasson K, Frigge ML, Kong A. Allegro, a new computer program for multipoint linkage analysis. Nat Genet 2000;25:12-13.
    • (2000) Nat Genet , vol.25 , pp. 12-13
    • Gudbjartsson, D.F.1    Jonasson, K.2    Frigge, M.L.3    Kong, A.4
  • 10
    • 0035960565 scopus 로고    scopus 로고
    • A new autosomal dominant pure cerebellar ataxia
    • Storey E, Gardner RJM, Knight MA, et al. A new autosomal dominant pure cerebellar ataxia. Neurol 2001;57:1913-1915.
    • (2001) Neurol , vol.57 , pp. 1913-1915
    • Storey, E.1    Gardner, R.J.M.2    Knight, M.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.