Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot–Marie–Tooth disease 4H

Charcot–Marie–Tooth (CMT) disease is one of the most common inherited neurological disorders, affecting either axons from the motor and/or sensory neurons or Schwann cells of the peripheral nervous system (PNS) and caused by more than 100 genes. We previously identified mutations in FGD4 as responsi...

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Detalles Bibliográficos
Autores principales: El-Bazzal, Lara, Ghata, Adeline, Estève, Clothilde, Gadacha, Jihane, Quintana, Patrice, Castro, Christel, Roeckel-Trévisiol, Nathalie, Lembo, Frédérique, Lenfant, Nicolas, Mégarbané, André, Borg, Jean-Paul, Lévy, Nicolas, Bartoli, Marc, Poitelon, Yannick, Roubertoux, Pierre L, Delague, Valérie, Bernard-Marissal, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10151191/
https://www.ncbi.nlm.nih.gov/pubmed/36314052
http://dx.doi.org/10.1093/brain/awac402

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