Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and...
Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review
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Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
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.
We compiled clinical data from a new Swedish kindred with R406W mutation. Seven family members were followed longitudinally for up to 22 years. Radiological...
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Full title
Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review
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TN_cdi_doaj_primary_oai_doaj_org_article_183914fe22824cb885cdc4f79908b05d
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_183914fe22824cb885cdc4f79908b05d
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ISSN
1758-9193
E-ISSN
1758-9193
DOI
10.1186/s13195-017-0330-2
