Schwann cells and the pathogenesis of inherited motor and sensory neuropathies (Charcot-Marie-Tooth disease)
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience,Neurology
Reference187 articles.
1. Heterozygous Peripheral Myelin Protein 22-Deficient Mice Are Affected by a Progressive Demyelinating Tomaculous Neuropathy
2. Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice
3. Analysis of compound heterozygous mice reveals that theTrembler mutation can behave as a gain-of-function allele
4. Peripheral Myelin Protein 22 Is in Complex with 6beta4 Integrin, and Its Absence Alters the Schwann Cell Basal Lamina
5. Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V
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