Abnormal Junctions and Permeability of Myelin in PMP22-Deficient Nerves

OBJECTIVE: The peripheral myelin protein-22 (PMP22) gene is associated with the most common types of inherited neuropathies, including hereditary neuropathy with liability to pressure palsies (HNPP) caused by PMP22 deficiency. However, the function of PMP22 has yet to be defined. Our previous study...

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Main Authors: Guo, Jiasong, Wang, Leiming, Zhang, Yang, Wu, Jiawen, Arpag, Sezgi, Hu, Bo, Imhof, Beat A., Tian, Xinxia, Carter, Bruce D., Suter, Ueli, Li, Jun
Format: Artigo
Jezik:Inglês
Izdano: 2014
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Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4206215/
https://ncbi.nlm.nih.gov/pubmed/24339129
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24086
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