Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia
Version of Record online: 22 JUN 2006
Copyright © 2006 Movement Disorder Society
Volume 21, Issue 9, pages 1531–1533, September 2006
How to Cite
Kaneko, S., Kawarai, T., Yip, E., Salehi-Rad, S., Sato, C., Orlacchio, A., Bernardi, G., Liang, Y., Hasegawa, H., Rogaeva, E. and St George-Hyslop, P. (2006), Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia. Mov. Disord., 21: 1531–1533. doi: 10.1002/mds.21005
- Issue online: 20 SEP 2006
- Version of Record online: 22 JUN 2006
- Manuscript Accepted: 13 MAR 2006
- Manuscript Revised: 31 JAN 2006
- Manuscript Received: 13 DEC 2005
- Canadian Institutes of Health Research
- Howard Hughes Medical Institute
- Parkinson Society of Canada
- Japan–Canada and Canadian Institutes of Health Research Joint Health Research Program
- Nakabayashi Trust
- Italian “Ministero della Salute”
- “Comitato Telethon Fondazione Onlus” (Italy). Grant Number: GGP030368
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