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Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland
BACKGROUND: Frontotemporal lobar degeneration (FTLD) consists of a clinically and neuropathologically heterogeneous group of syndromes affecting the frontal and temporal lobes of the brain. Mutations in microtubule-associated protein tau (MAPT), progranulin (PGRN) and charged multi-vesicular body pr...
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| 主要な著者: | , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2008
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2625345/ https://ncbi.nlm.nih.gov/pubmed/19091059 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-8-48 |
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