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Rer1 and calnexin regulate endoplasmic reticulum retention of a peripheral myelin protein 22 mutant that causes type 1A Charcot-Marie-Tooth disease

Peripheral myelin protein 22 (PMP22) resides in the plasma membrane and is required for myelin formation in the peripheral nervous system. Many PMP22 mutants accumulate in excess in the endoplasmic reticulum (ER) and lead to the inherited neuropathies of Charcot-Marie-Tooth (CMT) disease. However, t...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Hara, Taichi, Hashimoto, Yukiko, Akuzawa, Tomoko, Hirai, Rika, Kobayashi, Hisae, Sato, Ken
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4227013/
https://ncbi.nlm.nih.gov/pubmed/25385046
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep06992
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