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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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| Hoofdauteurs: | , , , , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2014
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| Onderwerpen: | |
| Online toegang: | 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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