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Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutations
OBJECTIVE: To identify clinicopathological differences between frontotemporal lobar degeneration (FTLD) due to mutations in progranulin (FTLD‐GRN) and chromosome 9 open reading frame 72 (FTLD‐C9ORF72). METHODS: We performed quantitative neuropathologic comparison of 17 FTLD‐C9ORF72 and 15 FTLD‐GRN w...
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| Publicado en: | Ann Clin Transl Neurol |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6764493/ https://ncbi.nlm.nih.gov/pubmed/31448566 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.50875 |
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