A rare intronic c.2654+1G>A mutation in CSF1R-microglial encephalopathy: a case report
ObjectiveWe report a case of CSF1R-microglial encephalopathy associated with a rare intronic c.2654 + 1G>A mutation, featuring negative diffusion-weighted imaging (DWI) findings and a cerebrospinal fluid (CSF) biomarker profile indicative of Alzheimer’s disease-related changes, and we explore the...
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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Frontiers Media S.A.
2025-08-01
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| Series: | Frontiers in Genetics |
| Assuntos: | |
| Acceso en liña: | https://www.frontiersin.org/articles/10.3389/fgene.2025.1593964/full |
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