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machado
/məˈʧɑdoʊ/
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joseph
/ˈʤoʊsəf/
disease
/dəˈziz/
Description
Machado-Joseph disease    autosomal dominant cerebellar ataxia that is characterized by slow degeneration of the hindbrain and has material basis in expansion of CAG triplet repeats (glutamine) in the ATXN3 gene

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