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PMP22 Is Critical for Actin-Mediated Cellular Functions and for Establishing Lipid Rafts
Haploinsufficiency of peripheral myelin protein 22 (PMP22) causes hereditary neuropathy with liability to pressure palsies, a peripheral nerve lesion induced by minimal trauma or compression. As PMP22 is localized to cholesterol-enriched membrane domains that are closely linked with the underlying a...
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| Publicado no: | J Neurosci |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Society for Neuroscience
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4244477/ https://ncbi.nlm.nih.gov/pubmed/25429154 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.1908-14.2014 |
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