Defective Glial Maturation in Vanishing White Matter Disease

Vanishing white matter disease (VWM) is a genetic leukoencephalopathy linked to mutations in the eukaryotic translation initiation factor 2B (eIF2B). It is a disease of infants, children and adults, who experience a slowly progressive neurological deterioration with episodes of rapid clinical worsen...

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Autors principals: Bugiani, Marianna, Boor, Ilja, van Kollenburg, Barbara, Postma, Nienke, Polder, Emiel, van Berkel, Carola, van Kesteren, Ronald E., Windrem, Martha S., Hol, Elly M., Scheper, Gert C., Goldman, Steven A., van der Knaap, Marjo S.
Format: Artigo
Idioma:Inglês
Publicat: 2011
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4135437/
https://ncbi.nlm.nih.gov/pubmed/21157376
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/NEN.0b013e318203ae74
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