Common neuropathological features underlie distinct clinical presentations in three siblings with hereditary diffuse leukoencephalopathy with spheroids caused by CSF1R p.Arg782His
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Title
Common neuropathological features underlie distinct clinical presentations in three siblings with hereditary diffuse leukoencephalopathy with spheroids caused by CSF1R p.Arg782His
Authors
Keywords
Leukoencephalopathy, Microglia, HDLS, <em class=EmphasisTypeItalic >CSF1R</em>, Frontotemporal degeneration, Corticobasal syndrome, Dementia with Lewy bodies
Journal
Acta Neuropathologica Communications
Volume 3, Issue 1, Pages -
Publisher
Springer Nature
Online
2015-07-03
DOI
10.1186/s40478-015-0219-x
References
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Related references
Note: Only part of the references are listed.- Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia linked CSF1R mutation: Report of four Korean cases
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- Hereditary diffuse leukoencephalopathy with axonal spheroids caused by R782H mutation in CSF1R: Case report
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- Neuropathology of Frontotemporal Lobar Degeneration-Tau (FTLD-Tau)
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