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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Detalles Bibliográficos
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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066968/
https://www.ncbi.nlm.nih.gov/pubmed/27749933
http://dx.doi.org/10.1371/journal.pone.0164617

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066968/
https://www.ncbi.nlm.nih.gov/pubmed/27749933
http://dx.doi.org/10.1371/journal.pone.0164617

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