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
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