Afferent Visual Pathway Affection in Patients with PMP22 Deletion-Related Hereditary Neuropathy with Liability to Pressure Palsies

BACKGROUND: The PMP22 gene encodes a protein integral to peripheral myelin. Its deletion leads to hereditary neuropathy with liability to pressure palsies (HNPP). PMP22 is not expressed in the adult central nervous system, but previous studies suggest a role in CNS myelin development. The objective...

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Detaylı Bibliyografya
Yayımlandı:PLoS One
Asıl Yazarlar: Brandt, Alexander U., Meinert-Bohn, Elena, Rinnenthal, Jan Leo, Zimmermann, Hanna, Mikolajczak, Janine, Oberwahrenbrock, Timm, Papazoglou, Sebastian, Pfüller, Caspar F., Schinzel, Johann, Tackenberg, Björn, Paul, Friedemann, Hahn, Katrin, Bellmann-Strobl, Judith
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2016
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5066968/
https://ncbi.nlm.nih.gov/pubmed/27749933
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0164617
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