| 1 | NOP56, SCA36
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| Characteristic RNA foci of the abnormal hexanucleotide GGCCUG repeat expansion in spinocerebellar ataxia type 36 (Asidan).
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| Liu W, Ikeda Y, Hishikawa N, Yamashita T, Deguchi K, Abe K.
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| Eur J Neurol ur J Neurol. 2014 Jul 2. doi: 10.1111/ene.12491. [Epub ahead of print]
2014
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| 2 | NOP56, SCA36
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| 'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterization.
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| García-Murias M, Quintáns B, Arias M, Seixas AI, Cacheiro P, Tarrío R, Pardo J, Millán MJ, Arias-Rivas S, Blanco-Arias P, Dapena D, Moreira R, Rodríguez-Trelles F, Sequeiros J, Carracedo A, Silveira I, Sobrido MJ.
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| Brain 135(Pt 5):1423-35. doi: 10.1093/brain/aws069. Epub 2012 Apr 3.
2012
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| 3 | NOP56, SCA36
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| Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement (Asidan).
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| Ikeda Y, Ohta Y, Kobayashi H, Okamoto M, Takamatsu K, Ota T, Manabe Y, Okamoto K, Koizumi A, Abe K.
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| Neurology 79(4):333-41. doi: 10.1212/WNL.0b013e318260436f. Epub 2012 Jun 27.
2012
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| 4 | NOP56, SCA36
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| Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.
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| Kobayashi H, Abe K, Matsuura T, Ikeda Y, Hitomi T, Akechi Y, Habu T, Liu W, Okuda H, Koizumi A.
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| Am J Hum Genet 89(1):121-30. doi: 10.1016/j.ajhg.2011.05.015. Epub 2011 Jun 16.
2011
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