1995•Journal of the Neurological SciencesRequires access

Spinocerebellar ataxia, type 3 (SCA3) is genetically identical to Machado-Joseph disease (MJD)

Gerd Haberhausen, Maxwell S. Damian, Frank Leweke, Ulrich Müller

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Key concepts: Machado–Joseph disease, Spinocerebellar ataxia, Trinucleotide repeat expansion, Genetics, Biology, Degenerative disease, Ataxia, Age of onset