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Volumn 50, Issue 4, 1996, Pages 199-201

Reduction of CAG expansions in cerebellar cortex and spinal cord of DRPLA

Author keywords

CAG repeats; Cerebellar cortex; DRPLA; Spinal cord

Indexed keywords

ARTICLE; CEREBELLUM CORTEX; CHROMOSOME 12; CLINICAL ARTICLE; DENTATORUBROPALLIDOLUYSIAN ATROPHY; HUMAN; NERVE CELL LESION; PERIPHERAL LYMPHOCYTE; PRIORITY JOURNAL; SPINAL CORD;

EID: 0030443297     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb02625.x     Document Type: Article
Times cited : (13)

References (12)
  • 2
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    • Aoki M, Ogasawara M, Matsubara Y, Narisawa K, Nakamura S, Itoyama Y, Abe K. Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible new subtype of familial ALS. J Neurol Sci 1994b: 126: 77-83.
    • (1994) J Neurol Sci , vol.126 , pp. 77-83
    • Aoki, M.1    Ogasawara, M.2    Matsubara, Y.3    Narisawa, K.4    Nakamura, S.5    Itoyama, Y.6    Abe, K.7
  • 3
    • 0029035710 scopus 로고
    • Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1
    • Chong SS, McCall AE, Cota J, Subramony SH, Orr HT, Hughes MR, Zoghbi HY. Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1. Nature Genet 1995: 10: 344-355.
    • (1995) Nature Genet , vol.10 , pp. 344-355
    • Chong, S.S.1    McCall, A.E.2    Cota, J.3    Subramony, S.H.4    Orr, H.T.5    Hughes, M.R.6    Zoghbi, H.Y.7
  • 7
    • 0020064620 scopus 로고
    • Familial myoclonus epilepsy and choreoathetosis: Hereditary dentatorubral-pallidoluysian atrophy
    • Naito H, Oyanagi S. Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy. Neurology 1982: 32: 798-807.
    • (1982) Neurology , vol.32 , pp. 798-807
    • Naito, H.1    Oyanagi, S.2
  • 10
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
    • The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 1993: 72: 971-983.
    • (1993) Cell , vol.72 , pp. 971-983
  • 12
    • 0029015557 scopus 로고
    • Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain
    • Yazawa I, Nukina N, Hashida H, Goto J, Yamada M, Kanazawa I. Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain. Nature Genet 1995: 10: 99-103.
    • (1995) Nature Genet , vol.10 , pp. 99-103
    • Yazawa, I.1    Nukina, N.2    Hashida, H.3    Goto, J.4    Yamada, M.5    Kanazawa, I.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.