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Fig. 1 | Acta Neuropathologica Communications

Fig. 1

From: Common neuropathological features underlie distinct clinical presentations in three siblings with hereditary diffuse leukoencephalopathy with spheroids caused by CSF1R p.Arg782His

Fig. 1

CSF1R protein domain and mutation schematic. Schematic diagram of the protein domain structure of CSF1R with amino acid numbers provided. Mutations previously reported in other studies are shown in black [3–5, 7–9] and the R782H mutation identified in the present study is highlighted in red. Ig: Immunoglobulin domains

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Acta Neuropathologica Communications

ISSN: 2051-5960

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