A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia

AIMS: Frontotemporal lobar degeneration (FTLD) is a progressive neurodegenerative disease and is the second most common form of young onset dementia after Alzheimer's disease (AD). An autosomal dominant pattern of inheritance is present in around 25–50% of FTLD cases indicating a strong genetic...

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Detalles Bibliográficos
Autores principales: Lashley, Tammaryn, Rohrer, Jonathan D, Mahoney, Colin, Gordon, Elizabeth, Beck, Jon, Mead, Simon, Warren, Jason, Rossor, Martin, Revesz, Tamas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260146/
https://www.ncbi.nlm.nih.gov/pubmed/24286341
http://dx.doi.org/10.1111/nan.12100

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260146/
https://www.ncbi.nlm.nih.gov/pubmed/24286341
http://dx.doi.org/10.1111/nan.12100

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