LETTER TO THE EDITOR
Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia
Article first published online: 4 APR 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 85, Issue 3, pages 296–297, March 2014
How to Cite
Maruyama, H., Morino, H., Miyamoto, R., Murakami, N., Hamano, T. and Kawakami, H. (2014), Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia. Clinical Genetics, 85: 296–297. doi: 10.1111/cge.12140
- Issue published online: 27 JAN 2014
- Article first published online: 4 APR 2013
- Manuscript Revised: 8 MAR 2013
- Manuscript Accepted: 8 MAR 2013
- Manuscript Received: 4 FEB 2013
- Cabinet Office of the Government of Japan
- Ministry of Education, Science, Sports and Culture of Japan
- Ministry of Health, Labour and Welfare of Japan
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