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HARVARD Citation
Maruyama, H. et al. (n.d.). Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia. Clinical genetics. pp. 296-297. [Online].
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Maruyama, H. et al. (n.d.). Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia. Clinical genetics. pp. 296-297. [Online].