Chargement en cours...

Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorder

Mutations in the gene of the peripheral myelin protein zero (P0) give rise to the peripheral neuropathies Charcot-Marie-Tooth type 1B disease (CMT1B), Déjérine-Sottas syndrome, and congenital hypomyelinating neuropathy. To investigate the pathomechanisms of a specific point mutation in the P0 gene,...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: Rünker, Annette E., Kobsar, Igor, Fink, Torsten, Loers, Gabriele, Tilling, Thomas, Putthoff, Peggy, Wessig, Carsten, Martini, Rudolf, Schachner, Melitta
Format: Artigo
Langue:Inglês
Publié: The Rockefeller University Press 2004
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2172360/
https://ncbi.nlm.nih.gov/pubmed/15148307
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.200402087
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!