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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Bibliografiska uppgifter
I publikationen:J Neurosci
Huvudupphovsmän: Lee, Sooyeon, Amici, Stephanie, Tavori, Hagai, Zeng, Waylon M., Freeland, Steven, Fazio, Sergio, Notterpek, Lucia
Materialtyp: Artigo
Språk:Inglês
Publicerad: Society for Neuroscience 2014
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Articles
Länkar: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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