These authors contributed equally to the work.
Autosomal Recessive Spinocerebellar Ataxia 7 (SCAR7) is Caused by Variants in TPP1, The Gene Involved in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis 2 Disease (CLN2 Disease)
Article first published online: 11 MAR 2013
© 2013 Wiley Periodicals, Inc.
Volume 34, Issue 5, pages 706–713, May 2013
How to Cite
Sun, Y., Almomani, R., Breedveld, G. J., Santen, G. W.E., Aten, E., Lefeber, D. J., Hoff, J. I., Brusse, E., Verheijen, F. W., Verdijk, R. M., Kriek, M., Oostra, B., Breuning, M. H., Losekoot, M., den Dunnen, J. T., van de Warrenburg, B. P. and Maat-Kievit, A. J.A. (2013), Autosomal Recessive Spinocerebellar Ataxia 7 (SCAR7) is Caused by Variants in TPP1, The Gene Involved in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis 2 Disease (CLN2 Disease). Hum. Mutat., 34: 706–713. doi: 10.1002/humu.22292
Additional Supporting Information may be found in the online version of this article.
Rowida Almomani's present address is Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Communicated by Prof. Christine Van Broeckhoven
Contract grant sponsors: EC's 7th Framework Programme (223026, 223143, 200754); China Scholarship Council.
- Issue published online: 11 APR 2013
- Article first published online: 11 MAR 2013
- Accepted manuscript online: 15 FEB 2013 11:29AM EST
- Manuscript Accepted: 31 JAN 2013
- Manuscript Received: 7 NOV 2012
- EC's 7th Framework Programme. Grant Numbers: 223026, 223143, 200754
- China Scholarship Council
Options for accessing this content:
- If you have access to this content through a society membership, please first log in to your society website.
- If you would like institutional access to this content, please recommend the title to your librarian.
- Login via other institutional login options http://onlinelibrary.wiley.com/login-options.
- You can purchase online access to this Article for a 24-hour period (price varies by title)
- If you already have a Wiley Online Library or Wiley InterScience user account: login above and proceed to purchase the article.
- New Users: Please register, then proceed to purchase the article.
Type your institution's name in the box below. If your institution is a Wiley customer, it will appear in the list of suggested institutions and you will be able to log in to access content. Some users may also log in directly via OpenAthens.
Please note that there are currently a number of duplicate entries in the list of institutions. We are actively working on fixing this issue and apologize for any inconvenience caused.
Registered Users please login:
- Access your saved publications, articles and searches
- Manage your email alerts, orders and subscriptions
- Change your contact information, including your password
Please register to:
- Save publications, articles and searches
- Get email alerts
- Get all the benefits mentioned below!