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Peripheral myelin protein 22 alters membrane architecture

Peripheral myelin protein 22 (PMP22) is highly expressed in myelinating Schwann cells of the peripheral nervous system. PMP22 genetic alterations cause the most common forms of Charcot-Marie-Tooth disease (CMTD), which is characterized by severe dysmyelination in the peripheral nerves. However, the...

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Detalles Bibliográficos
Autores principales: Mittendorf, Kathleen F., Marinko, Justin T., Hampton, Cheri M., Ke, Zunlong, Hadziselimovic, Arina, Schlebach, Jonathan P., Law, Cheryl L., Li, Jun, Wright, Elizabeth R., Sanders, Charles R., Ohi, Melanie D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498104/
https://www.ncbi.nlm.nih.gov/pubmed/28695207
http://dx.doi.org/10.1126/sciadv.1700220