Molecular diagnosis of Charcot–Marie–Tooth disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical)
Link
http://www.nature.com/articles/nrneurol.2011.72.pdf
Reference8 articles.
1. Pareyson, D. & Marchesi, C. Diagnosis, natural history, and management of Charcot–Marie–Tooth disease. Lancet Neurol. 8, 654–667 (2009).
2. Harding, A. E. From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins. Brain 118, 809–818 (1995).
3. Saporta, A. S. et al. Charcot–Marie–Tooth disease subtypes and genetic testing strategies. Ann. Neurol. 69, 22–33 (2011).
4. Amato, A. A. & Reilly, M. M. The death panel for Charcot–Marie–Tooth panels. Ann. Neurol. 69, 1–4 (2011).
5. England, J. D. et al. Practice Parameter: evaluation of distal symmetric polyneuropathy: role of autonomic testing, nerve biopsy, and skin biopsy (an evidence-based review). Report of the American Academy of Neurology, American Association of Neuromuscular and Electrodiagnostic Medicine, and American Academy of Physical Medicine and Rehabilitation. Neurology 72, 177–184 (2009).
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