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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2015
Materias:
New Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603256/
https://www.ncbi.nlm.nih.gov/pubmed/26478912
http://dx.doi.org/10.1523/ENEURO.0080-15.2015

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603256/
https://www.ncbi.nlm.nih.gov/pubmed/26478912
http://dx.doi.org/10.1523/ENEURO.0080-15.2015

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