Our patient material included families and sporadic patients of Finnish origin with the diagnosis of Charcot-Marie-Tooth (CMT) disease types 1 and 2, Dejerine-Sottas syndrome (DSS), and hereditary neuropathy with liability to pressure palsies (HNPP). We screened for mutations in the peripheral myeli
✦ LIBER ✦
How to assess the pathogenicity of mutations in Charcot-Marie-Tooth disease and other diseases?
✍ Scribed by Andrzej Kochański
- Publisher
- Springer-Verlag
- Year
- 2006
- Tongue
- English
- Weight
- 77 KB
- Volume
- 47
- Category
- Article
- ISSN
- 1234-1983
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