Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy
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Article Information
- Received October 18, 2011
- Accepted January 23, 2012
- First Published May 9, 2012.
Article Versions
- Previous version (May 9, 2012 - 13:02).
- You are viewing the most recent version of this article.
Author Disclosures
- Z. Zhao, MS,
- A. Hashiguchi, MD,
- J. Hu, MD, PhD,
- Y. Sakiyama, MD, PhD,
- Y. Okamoto, MD, PhD,
- S. Tokunaga, MD,
- L. Zhu, MB,
- H. Shen, MS and
- H. Takashima, MD, PhD
- Z. Zhao, MS,
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- A. Hashiguchi, MD,
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- J. Hu, MD, PhD,
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- Y. Sakiyama, MD, PhD,
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- Y. Okamoto, MD, PhD,
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- S. Tokunaga, MD,
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- L. Zhu, MB,
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- H. Shen, MS and
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- H. Takashima, MD, PhD
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Received speaker honoraria from Kyushu University, GlaxoSmithKline, Bayer, Eisaico., Novartis, Tanabe Mitsubishi, Biogen Idec, Benesis co., Takeda, Teijin, Pfizer, and Dainippon Sumitomo Pharma
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Receive consulting fees from Teijin;
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Funded by the Japanese Ministry of Health, Welfare, and Labor Research Committee for Charcot–Marie–Tooth Disease (2010-present), Ataxic disease; , Applying Health Technology; , the Ministry of Education, Culture, Sports, Science, and Technology of Japan. government granting agency grant 21591095(2009-present)
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Royalty from the Athena diagnostics (2003-present)
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- From the Departments of Neuromuscular Disease (Z.Z., J.H., H.S.) and Electromyography (L.Z.), Third Hospital of Hebei Medical University, Shijiazhuang, PR China; and Department of Neurology and Geriatrics (A.H., Y.S., Y.O., S.T., H.T.), Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
- Correspondence & reprint requests to Dr. Hu: jinghujp{at}yahoo.com.cn
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