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Microglia express ABI3 in the brains of Alzheimer's disease and Nasu-Hakola disease
Nasu-Hakola disease (NHD) is a rare autosomal recessive leukoencephalopathy caused by a loss-of-function mutation of either TYROBP (DAP12) or TREM2 expressed in microglia. A rare variant of the TREM2 gene encoding p.Arg47His causes a 3-fold increase in the risk for late-onset Alzheimer's diseas...
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| Publicado en: | Intractable Rare Dis Res |
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| Autores principales: | , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5735279/ https://ncbi.nlm.nih.gov/pubmed/29259854 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2017.01073 |
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