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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Veröffentlicht in:Neurology
Hauptverfasser: Konno, Takuya, Kasanuki, Koji, Ikeuchi, Takeshi, Dickson, Dennis W., Wszolek, Zbigniew K.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Lippincott Williams & Wilkins 2018
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Online Zugang: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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