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Volumn 345, Issue 2, 2003, Pages 93-96

Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India

Author keywords

CA150 locus; GluR6 locus; Huntington's disease; Modifiers; RAI1 locus; SCA2

Indexed keywords

HUNTINGTIN;

EID: 0038042172     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0304-3940(03)00436-1     Document Type: Article
Times cited : (56)

References (12)
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    • Basu P., Chattopadhyay B., Gangopadhyay P.K., Mukherjee S.C., Sinha K.K., Das S.K., Roychoudhury S.C., Majumder P.P., Bhattacharyya N.P. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine populations of eastern India. Hum. Genet. 106:2000;597-604.
    • (2000) Hum. Genet. , vol.106 , pp. 597-604
    • Basu, P.1    Chattopadhyay, B.2    Gangopadhyay, P.K.3    Mukherjee, S.C.4    Sinha, K.K.5    Das, S.K.6    Roychoudhury, S.C.7    Majumder, P.P.8    Bhattacharyya, N.P.9
  • 4
    • 0030795968 scopus 로고    scopus 로고
    • The CAG/polyglutamine tract diseases: Gene products and molecular pathogenesis
    • Koshy B.T., Zoghbi H.Y. The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis. Brain Pathol. 7:1997;927-942.
    • (1997) Brain Pathol. , vol.7 , pp. 927-942
    • Koshy, B.T.1    Zoghbi, H.Y.2
  • 6
    • 0037008355 scopus 로고    scopus 로고
    • Mutation analysis and association studies of the ubiquitin carboxy-terminal hydrolase L1 gene in Huntington's disease
    • Naze P., Vuillaume I., Destee A., Pasquier F., Sablonniere B. Mutation analysis and association studies of the ubiquitin carboxy-terminal hydrolase L1 gene in Huntington's disease. Neurosci. Lett. 328:2002;1-4.
    • (2002) Neurosci. Lett. , vol.328 , pp. 1-4
    • Naze, P.1    Vuillaume, I.2    Destee, A.3    Pasquier, F.4    Sablonniere, B.5
  • 8
    • 0030937818 scopus 로고    scopus 로고
    • Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington's disease
    • Rubinsztein D.C., Leggo J., Chiano M., Dodge A., Norbury G., Rosser E., Craufurd D. Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington's disease. Proc. Natl. Acad. Sci. USA. 94:1997;3872-3876.
    • (1997) Proc. Natl. Acad. Sci. USA , vol.94 , pp. 3872-3876
    • Rubinsztein, D.C.1    Leggo, J.2    Chiano, M.3    Dodge, A.4    Norbury, G.5    Rosser, E.6    Craufurd, D.7
  • 12
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosome
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosome. Cell. 72:1993;971-983.
    • (1993) Cell , vol.72 , pp. 971-983


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.