Charcot-Marie-Tooth type 1B (CMT 1B) disease, an inherited demyelinating peripheral neuropathy, results from different point mutations located in the P0 gene on chromosome 1 q21-23. We have quantified, at the ultrastructural level, the immunocytochemical expression of the P0 protein in two unrelated
Diagnostic nerve ultrasound in Charcot–Marie–Tooth disease type 1B
✍ Scribed by Michael S. Cartwright; Martin E. Brown; Patrick Eulitt; Francis O. Walker; Victoria H. Lawson; James B. Caress
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 100 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0148-639X
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