CSF and Blood Levels of GFAP in Alexander Disease

Alexander disease is a rare, progressive, and generally fatal neurological disorder that results from dominant mutations affecting the coding region of GFAP, the gene encoding glial fibrillary acidic protein, the major intermediate filament protein of astrocytes in the CNS. A key step in pathogenesi...

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Bibliografski detalji
Izdano u:eNeuro
Glavni autori: Jany, Paige L., Agosta, Guillermo E., Benko, William S., Eickhoff, Jens C., Keller, Stephanie R., Köehler, Wolfgang, Koeller, David, Mar, Soe, Naidu, Sakkubai, Marie Ness, Jayne, Pareyson, Davide, Renaud, Deborah L., Salsano, Ettore, Schiffmann, Raphael, Simon, Julie, Vanderver, Adeline, Eichler, Florian, van der Knaap, Marjo S., Messing, Albee
Format: Artigo
Jezik:Inglês
Izdano: Society for Neuroscience 2015
Teme:
New Research
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4603256/
https://ncbi.nlm.nih.gov/pubmed/26478912
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/ENEURO.0080-15.2015
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