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CSF1R-related leukoencephalopathy: A major player in primary microgliopathies
Since the discovery of CSF1R gene mutations in families with hereditary diffuse leukoencephalopathy with spheroids in 2012, more than 70 different mutations have been identified around the world. Through the analyses of mutation carriers, CSF1R-related leukoencephalopathy has been distinctly charact...
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| Publicat a: | Neurology |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Lippincott Williams & Wilkins
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6329328/ https://ncbi.nlm.nih.gov/pubmed/30429277 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000006642 |
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