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- Kawaguchi Y., Okamoto T., Taniwaki M., Aizawa M., Inoue M., Katayama S., Kawakami H., Nakamura S., Nishimura M., Akiguchi I. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat Genet. 1994 Nov;8(3):221–228. doi: 10.1038/ng1194-221. [DOI] [PubMed] [Google Scholar]
- Matilla T., McCall A., Subramony S. H., Zoghbi H. Y. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease. Ann Neurol. 1995 Jul;38(1):68–72. doi: 10.1002/ana.410380113. [DOI] [PubMed] [Google Scholar]
- Sakai T., Kawakami H. Machado-Joseph disease: A proposal of spastic paraplegic subtype. Neurology. 1996 Mar;46(3):846–847. [PubMed] [Google Scholar]
- Schöls L., Vieira-Saecker A. M., Schöls S., Przuntek H., Epplen J. T., Riess O. Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients. Hum Mol Genet. 1995 Jun;4(6):1001–1005. doi: 10.1093/hmg/4.6.1001. [DOI] [PubMed] [Google Scholar]