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Unfolded protein response, treatment and CMT1B

CMT1B is the second most frequent autosomal dominant inherited neuropathy and is caused by assorted mutations of the myelin protein zero (MPZ) gene. MPZ mutations cause neuropathy gain of function mechanisms that are largely independent MPZs normal role of mediating myelin compaction. Whether there...

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Detalhes bibliográficos
Main Authors: Bai, Yunhong, Patzko, Agnes, Shy, Michael E.
Formato: Artigo
Idioma:Inglês
Publicado em: Landes Bioscience 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3915562/
https://ncbi.nlm.nih.gov/pubmed/25002989
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/rdis.24049
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