Presymptomatic studies in genetic frontotemporal dementia

Approximately 20% of patients with the neurodegenerative disorder frontotemporal dementia (FTD) have an autosomal dominant pattern of inheritance. Genetic FTD is caused by mutations in three genes in most cases (progranulin, microtubule-associated protein tau and chromosome 9 open reading frame 72)...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Rohrer, J.D., Warren, J.D., Fox, N.C., Rossor, M.N.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Masson 2013
Pynciau:
International meeting of the French society of neurology 2013
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3878569/
https://ncbi.nlm.nih.gov/pubmed/24012408
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurol.2013.07.010
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