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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Библиографические подробности
Опубликовано в: :eNeuro
Главные авторы: 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
Формат: Artigo
Язык:Inglês
Опубликовано: Society for Neuroscience 2015
Предметы:
New Research
Online-ссылка: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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