Literature DB >> 16311891

Unexpected clinicopathological phenotype linked to small elongation of CAG repeat in SCA1 gene.

T Uchihara, Y Takeda, T Kobayashi, T Kasuga, K Ishikawa, K Kirei, H Mizusawa, T Endo, K Hirokawa, T Kuroiwa.   

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Year:  2005        PMID： 16311891     DOI： 10.1007/s00415-005-0980-z

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  4 in total

1.  Letter: Hereditary ataxia and HL-A genotypes.

Authors:  H Yakura; A Wakisaka; S Fujimoto; K Itakura
Journal:  N Engl J Med       Date:  1974-07-18       Impact factor: 91.245

Review 2.  Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations.

Authors:  K Iwabuchi; K Tsuchiya; T Uchihara; S Yagishita
Journal:  Rev Neurol (Paris)       Date:  1999-04       Impact factor: 2.607

3.  Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

Authors:  H T Orr; M Y Chung; S Banfi; T J Kwiatkowski; A Servadio; A L Beaudet; A E McCall; L A Duvick; L P Ranum; H Y Zoghbi
Journal:  Nat Genet       Date:  1993-07       Impact factor: 38.330

4.  Nuclear inclusions in spinocerebellar ataxia type 1.

Authors:  C Duyckaerts; A Dürr; G Cancel; A Brice
Journal:  Acta Neuropathol       Date:  1999-02       Impact factor: 17.088
  4 in total

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