Phenotypic Variation of Autosomal-Dominant Corticobasal Degeneration

Neurodegenerative tauopathies may be inherited as autosomal-dominant disorders with variable clinicopathological phenotypes, and causative mutations in the microtubule-associated protein tau (MAPT) gene are not regularly seen. Herein, we describe a patient with clinically typical and autopsy-proven...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: H. Jung, Hans, Bremer, Juliane, Streffer, Johannes, Virdee, Kanwar, Grazia Spillantini, Maria, Anthony Crowther, R., Brugger, Peter, Van Broeckhoven, Christine, Aguzzi, Adriano, Tolnay, Markus
Natura: Artigo
Lingua:Inglês
Pubblicazione: S. Karger AG 2012
Soggetti:
Neurologic Image
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3638994/
https://ncbi.nlm.nih.gov/pubmed/22261560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000334731
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi