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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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Podrobná bibliografie
Vydáno v:Neurology
Hlavní autoři: Konno, Takuya, Kasanuki, Koji, Ikeuchi, Takeshi, Dickson, Dennis W., Wszolek, Zbigniew K.
Médium: Artigo
Jazyk:Inglês
Vydáno: Lippincott Williams & Wilkins 2018
Témata:
On-line přístup: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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