E-mail

E-mail a Wiley Online Library Link

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

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field

SEARCH