Genotype–phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene

We aimed to characterize genotype–phenotype correlations and establish baseline clinical data for peripheral neuropathies caused by mutations in the myelin protein zero (MPZ) gene. MPZ mutations are the second leading cause of Charcot–Marie–Tooth disease type 1. Recent research makes clinical trials...

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Detalhes bibliográficos
Publicado no:Brain
Main Authors: Sanmaneechai, Oranee, Feely, Shawna, Scherer, Steven S., Herrmann, David N., Burns, Joshua, Muntoni, Francesco, Li, Jun, Siskind, Carly E., Day, John W., Laura, Matilde, Sumner, Charlotte J., Lloyd, Thomas E., Ramchandren, Sindhu, Shy, Rosemary R., Grider, Tiffany, Bacon, Chelsea, Finkel, Richard S., Yum, Sabrina W., Moroni, Isabella, Piscosquito, Giuseppe, Pareyson, Davide, Reilly, Mary M., Shy, Michael E.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2015
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4643641/
https://ncbi.nlm.nih.gov/pubmed/26310628
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awv241
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