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CSF1R Mutation p.G589R and the Distribution Pattern of Brain Calcification
We herein report the case of a 47-year-old female with the colony-stimulating factor 1 receptor (CSF1R) mutation p.G589R, which is related to hereditary leukoencephalopathy with axonal spheroid (HDLS). The patient presented with an early-onset cognitive decline and progressive aphasia. Brain magneti...
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| Publicat a: | Intern Med |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Japanese Society of Internal Medicine
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5643183/ https://ncbi.nlm.nih.gov/pubmed/28824062 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2169/internalmedicine.8462-16 |
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