Funding agencies: This study was supported by the Friedreich Ataxia Research Association (Australasia), Friedreich Ataxia Research Alliance (USA), Muscular Dystrophy Association, Australian Rotary Health Fund, and Collier Charitable Fund as well as the Victorian State Government Operational Infrastructure Support and Australian Government NHMRC IRIISS.
HFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxia
Article first published online: 3 JAN 2014
© 2013 International Parkinson and Movement Disorder Society
Volume 29, Issue 7, pages 940–943, June 2014
How to Cite
Delatycki, M. B., Tai, G., Corben, L., Yiu, E. M., Evans-Galea, M. V., Stephenson, S. E.M., Gurrin, L., Allen, K. J., Lynch, D. and Lockhart, P. J. (2014), HFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxia. Mov. Disord., 29: 940–943. doi: 10.1002/mds.25795
Relevant conflicts of interest/financial disclosures: Martin B. Delatycki is a Practitioner Fellow, Louise Corben is an Early Career Fellow, and Lyle Gurrin and Paul J. Lockhart are Career Development Fellows all of the National Health and Medical Research Council. Katrina J. Allen is a Viertel Senior Medical Research Fellow.
Full financial disclosures and author roles may be found in the online version of this article.
- Issue published online: 12 JUN 2014
- Article first published online: 3 JAN 2014
- Manuscript Accepted: 3 DEC 2013
- Manuscript Revised: 26 NOV 2013
- Manuscript Received: 27 JUL 2013
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