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Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation
BACKGROUND: The Arg406Trp (R406W) missense mutation in the microtubule associated protein-tau gene (MAPT) is a known cause of early-onset dementia (EOD). Various dementia phenotypes have been described, including frontotemporal dementia (FTD), FTD with Parkinsonism, and early-onset Alzheimer Disease...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3762928/ https://ncbi.nlm.nih.gov/pubmed/23727082 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jalz.2013.02.011 |
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