Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review

BACKGROUND: The MAPT c.1216C > T (p.Arg406Trp; R406W) mutation is a known cause of frontotemporal dementia with Parkinsonism linked to chromosome 17 tau with Alzheimer’s disease-like clinical features. METHODS: We compiled clinical data from a new Swedish kindred with R406W mutation. Seven family...

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Detalles Bibliográficos
Autores principales: Ygland, Emil, van Westen, Danielle, Englund, Elisabet, Rademakers, Rosa, Wszolek, Zbigniew K., Nilsson, Karin, Nilsson, Christer, Landqvist Waldö, Maria, Alafuzoff, Irina, Hansson, Oskar, Gustafson, Lars, Puschmann, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389050/
https://www.ncbi.nlm.nih.gov/pubmed/29370822
http://dx.doi.org/10.1186/s13195-017-0330-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389050/
https://www.ncbi.nlm.nih.gov/pubmed/29370822
http://dx.doi.org/10.1186/s13195-017-0330-2

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