Autosomal-dominant cerebellar ataxias
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Publisher
Elsevier
Reference84 articles.
1. Striatal and nigral pathology in a lentiviral rat model of Machado-Joseph disease;Alves;Hum Mol Genet 2008,2008
2. Silencing ataxin-3 mitigates degeneration in a rat model of Machado-Joseph disease: no role for wild-type ataxin-3?;Alves;Hum Mol Genet,2010
3. Mutant β-III spectrin causes mGluR1α mislocalization and functional deficits in a mouse model of spinocerebellar ataxia type 5;Armbrust;J Neurosci,2014
4. Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23;Bakalkin;Am J Hum Genet,2010
5. Reversibility of symptoms in a conditional mouse model of spinocerebellar ataxia type 3;Boy;Hum Mol Genet,2009
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