We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleThe Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotypeAuthorsDe Jonghe, P.; Timmerman, V.; Ceuterick, C.; Nelis, E.; De Vriendt, E.; Löfgren, A.; Vercruyssen, A.; Verellen, C.; Van Maldergem, L.; Martin, J.-J.; Van Broeckhoven, C.PublicationBrain, 1999, Vol 122, Issue 2, p281ISSN0006-8950Publication typearticleDOI10.1093/brain/122.2.281