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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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Detalles Bibliográficos
Autores principales:	Daida, Kensuke, Nishioka, Kenya, Li, Yuanzhe, Nakajima, Sho, Tanaka, Ryota, Hattori, Nobutaka
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Japanese Society of Internal Medicine 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643183/ https://www.ncbi.nlm.nih.gov/pubmed/28824062 http://dx.doi.org/10.2169/internalmedicine.8462-16

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