Hereditary motor and sensory neuropathies (HMSN) comprises a wide clinical spectrum of related disorders with defects in peripheral nerve myelination. Charcot-Marie-Tooth type 1 (CMT1) is the most common form and is usually a mild disease with onset in the first or second decade; however there is a
✦ LIBER ✦
Adult onset charcot–marie–tooth disease type 1d with an Arg381Cys mutation of EGR2
✍ Scribed by Chiara Briani; Federica Taioli; Marta Lucchetta; Roberto Bombardi; Gian Maria Fabrizi
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 223 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0148-639X
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