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• W1873606312 abstract "Clinical GeneticsVolume 85, Issue 3 p. 296-297 LETTER TO THE EDITOR Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia H. Maruyama, Corresponding Author H. Maruyama Department of Epidemiology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan Correspondence: Hirofumi Maruyama, MD, PhD Department of Epidemiology Research Institute for Radiation Biology and Medicine Hiroshima University 1-2-3, Kasumi, Minami-ku Hiroshima 734-8553 Japan Tel.: +81 82 2575847 Fax: +81 82 2575848 e-mail: hmaru@hiroshima-u.ac.jpSearch for more papers by this authorH. Morino, H. Morino Department of Epidemiology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, JapanSearch for more papers by this authorR. Miyamoto, R. Miyamoto Department of Epidemiology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, JapanSearch for more papers by this authorN. Murakami, N. Murakami Department of Neurology, Kansai Electric Power Hospital, Osaka, JapanSearch for more papers by this authorT. Hamano, T. Hamano Department of Neurology, Kansai Electric Power Hospital, Osaka, JapanSearch for more papers by this authorH. Kawakami, H. Kawakami Department of Epidemiology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, JapanSearch for more papers by this author H. Maruyama, Corresponding Author H. Maruyama Department of Epidemiology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan Correspondence: Hirofumi Maruyama, MD, PhD Department of Epidemiology Research Institute for Radiation Biology and Medicine Hiroshima University 1-2-3, Kasumi, Minami-ku Hiroshima 734-8553 Japan Tel.: +81 82 2575847 Fax: +81 82 2575848 e-mail: hmaru@hiroshima-u.ac.jpSearch for more papers by this authorH. Morino, H. Morino Department of Epidemiology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, JapanSearch for more papers by this authorR. Miyamoto, R. Miyamoto Department of Epidemiology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, JapanSearch for more papers by this authorN. Murakami, N. Murakami Department of Neurology, Kansai Electric Power Hospital, Osaka, JapanSearch for more papers by this authorT. Hamano, T. Hamano Department of Neurology, Kansai Electric Power Hospital, Osaka, JapanSearch for more papers by this authorH. Kawakami, H. Kawakami Department of Epidemiology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, JapanSearch for more papers by this author First published: 04 April 2013 https://doi.org/10.1111/cge.12140Citations: 17Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article.Citing Literature Volume85, Issue3March 2014Pages 296-297 RelatedInformation" @default.
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• W1873606312 title "Exome sequencing reveals a novel <i> <scp>ANO10</scp> </i> mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia" @default.
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