Potential conflict of interest: None reported.
A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype–phenotype correlations†
Version of Record online: 31 DEC 2008
Copyright © 2008 Movement Disorder Society
Volume 24, Issue 3, pages 441–445, 15 February 2009
How to Cite
Kubota, A., Hida, A., Ichikawa, Y., Momose, Y., Goto, J., Igeta, Y., Hashida, H., Yoshida, K., Ikeda, S.-I., Kanazawa, I. and Tsuji, S. (2009), A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype–phenotype correlations. Mov. Disord., 24: 441–445. doi: 10.1002/mds.22435
- Issue online: 23 FEB 2009
- Version of Record online: 31 DEC 2008
- Manuscript Accepted: 17 NOV 2008
- Manuscript Revised: 21 OCT 2008
- Manuscript Received: 1 JUL 2008
- KAKENHI (Grant-in-Aid for Scientific Research)
- Priority Areas, Applied Genomics
- 21st Century COE Program
- Center for Integrated Brain Medical Science
- Scientific Research (A)
- Ministry of Education, Culture, Sports, and Science
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