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)...

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Detalles Bibliográficos
Autores principales: Rohrer, J.D., Warren, J.D., Fox, N.C., Rossor, M.N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Masson 2013
Materias:
International meeting of the French society of neurology 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878569/
https://www.ncbi.nlm.nih.gov/pubmed/24012408
http://dx.doi.org/10.1016/j.neurol.2013.07.010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878569/
https://www.ncbi.nlm.nih.gov/pubmed/24012408
http://dx.doi.org/10.1016/j.neurol.2013.07.010

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