The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family

Multiple system tauopathy with presenile dementia (MSTD) is an inherited disease caused by a (g) to (a) transition at position +3 in intron 10 of Tau. It belongs to the spectrum of frontotemporal dementia and parkinsonism linked to chromosome 17 with mutations in Tau (FTDP-17T). Here we present the...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: Spina, Salvatore, Farlow, Martin R., Unverzagt, Frederick W., Kareken, David A., Murrell, Jill R., Fraser, Graham, Epperson, Francine, Crowther, R. Anthony, Spillantini, Maria G., Goedert, Michel, Ghetti, Bernardino
Format: Artigo
Langue:Inglês
Publié: Oxford University Press 2008
Sujets:
Original Articles
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2702832/
https://ncbi.nlm.nih.gov/pubmed/18065436
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awm280
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires