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H. Maruyama, H. Morino, R. Miyamoto, N. Murakami, T. Hamano and H. Kawakami Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia Clinical Genetics 85

Version of Record online: 4 APR 2013 | DOI: 10.1111/cge.12140

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