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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Publicado en:PLoS One
Autores principales: 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
Formato: Artigo
Lenguaje:Inglês
Publicado: Public Library of Science 2016
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Research Article
Acceso en línea: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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