Article PDF
Avoid common mistakes on your manuscript.
References
Duyckaerts C, Dürr A, Cancel G, Brice A (1999) Nuclear inclusions in spinocerebellar ataxia type 1. Acta Neuropathol (Berl) 97:201–207
Iwabuchi K, Tsuchiya K, Uchihara T, Yagishita S (1999) Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations. Rev Neurol (Paris) 155:255–270
Koyano S, Iwabuchi K, Yagishita S, Kuroiwa Y, Uchihara T (2002) Paradoxical absence of nuclear inclusion in cerebellar Purkinje cells of hereditary ataxias linked to CAG expansion. J Neurol Neurosurg. Psychiatry 73:453–455
Orr HT, Chung MY, Banfi S, Kwiatkowski TJ Jr, Servadio A, Beaudet AL, McCall AE, Duvick LA, Ranum LP, Zoghbi HY (1993) Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet 4:221–226
Yakura H, Wakisaka A, Fujimoto S, Itakura K (1974) Hereditary ataxia and HLA genotype. N Engl J Med 291:154–155
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Uchihara, T., Takeda, Y., Kobayashi, T. et al. Unexpected clinicopathological phenotype linked to small elongation of CAG repeat in SCA1 gene. J Neurol 253, 396–398 (2006). https://doi.org/10.1007/s00415-005-0980-z
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00415-005-0980-z