See editorial by Meschia on page 3.
p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese males
Version of Record online: 31 MAY 2013
© 2013 The Author(s) European Journal of Neurology © 2013 EFNS
European Journal of Neurology
Volume 21, Issue 1, pages 49–56, January 2014
How to Cite
Nakamura, K., Sekijima, Y., Nakamura, K., Hattori, K., Nagamatsu, K., Shimizu, Y., Yazaki, M., Sakurai, A., Endo, F., Fukushima, Y. and Ikeda, S.-I. (2014), p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese males. European Journal of Neurology, 21: 49–56. doi: 10.1111/ene.12214
- Issue online: 10 DEC 2013
- Version of Record online: 31 MAY 2013
- Manuscript Accepted: 30 APR 2013
- Manuscript Received: 14 MAR 2013
- Japanese Society for the Promotion of Science and Ministry of Education, Culture, Sports, Science and Technology
- Ministry of Health, Labor and Welfare
|ene12214-sup-0001-FigureS1.pdf||application/PDF||82K||Figure S1. Pedigrees of patients with p.E66Q mutation.|
Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.