Young‐onset frontotemporal dementia in a homozygous tau R406W mutation carrier

Microtubule‐associated protein tau mutations result in 10–20% of cases of genetic frontotemporal lobar degeneration. Tau mutation carriers typically develop behavioral variant frontotemporal dementia with or without parkinsonism. Unlike most frontotemporal dementia gene mutations, heterozygous R406W...

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Detalles Bibliográficos
Autores principales: Ng, Adeline S. L., Sias, Ana C., Pressman, Peter S., Fong, Jamie C., Karydas, Anna M., Zanto, Theodore P., De May, Mary, Coppola, Giovanni, Geschwind, Daniel H., Miller, Bruce L., Lee, Suzee E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693591/
https://www.ncbi.nlm.nih.gov/pubmed/26734663
http://dx.doi.org/10.1002/acn3.265

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693591/
https://www.ncbi.nlm.nih.gov/pubmed/26734663
http://dx.doi.org/10.1002/acn3.265

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