These authors contributed equally to this manuscript.
C9ORF72 Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease
Article first published online: 12 JUL 2013
© 2013 The Authors. Annals of Human Genetics published by John Wiley & Sons Ltd/University College London
This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
Annals of Human Genetics
Volume 77, Issue 5, pages 351–363, September 2013
How to Cite
Nuytemans, K., Bademci, G., Kohli, M. M., Beecham, G. W., Wang, L., Young, J. I., Nahab, F., Martin, E. R., Gilbert, J. R., Benatar, M., Haines, J. L., Scott, W. K., Züchner, S., Pericak-Vance, M. A. and Vance, J. M. (2013), C9ORF72 Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease. Annals of Human Genetics, 77: 351–363. doi: 10.1111/ahg.12033
- Issue published online: 6 AUG 2013
- Article first published online: 12 JUL 2013
- Manuscript Accepted: 4 JUN 2013
- Manuscript Received: 7 NOV 2012
- National Institute of Health. Grant Numbers: NS39764, 5P50NS071674-03, R01AG019085, R01AG027944-02, R01AG028786-02, RC2AG036528, U01AG032984-02
- Alzheimer's Association
- American Health Assistance Foundation
Disclaimer: Supplementary materials have been peer-reviewed but not copyedited.
Haplotype analysis in intermediate carriers and pedigrees displaying segregation analysis in families 2–9 can be found online.
Table S1 Analysis of 20 SNP risk haplotype in C9ORF72 intermediate repeat carriers.
Figure S1 Segregation analysis in Family 2.
Figure S2 Segregation analysis in Family 3.
Figure S3 Segregation analysis in Family 4.
Figure S4 Segregation analysis in Family 5.
Figure S5 Segregation analysis in Family 6.
Figure S6 Segregation analysis in Family 7.
Figure S7 Segregation analysis in Family 8.
Figure S8 Segregation analysis in Family 9.
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