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Japanese Familial Cases of Frontotemporal Dementia and Parkinsonism with N279K Tau Gene Mutation
BACKGROUND: Mutations in the tau gene linked to chromosome 17 cause frontotemporal dementia and parkinsonism (FTDP‐17). OBJECTIVE: This study presents 3 Japanese familial cases diagnosed with N279K tau gene mutation, including 1 autopsy‐confirmed case. METHODS: We compared the clinical presentations...
Shranjeno v:
| izdano v: | Mov Disord Clin Pract |
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| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
John Wiley & Sons, Inc.
2020
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7780954/ https://ncbi.nlm.nih.gov/pubmed/33426168 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.13100 |
| Oznake: |
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