Evidence for macrophage-mediated myelin
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Igor Kobsar; Kerstin Hasenpusch-Theil; Carsten Wessig; Hans Werner MΓΌller; Rudol
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Article
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2005
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John Wiley and Sons
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English
β 227 KB
## Abstract CharcotβMarieβTooth neuropathy type 1A (CMT1A) is the most common inherited neuropathy in humans and is mostly caused by a 1.5βMb tandem duplication of chromosome 17 comprising the gene for the peripheral myelin protein 22βkDa (PMP22). Although there are numerous studies on the function