A Novel Mutation of GFAP Causing Adult-Onset Alexander Disease

Alexander disease (AxD) is a rare, autosomal dominant neurological disorder. Three clinical subtypes are distinguished based on age at onset: infantile (0–2 years), juvenile (2–13 years), and adult (>13 years). The three forms differ in symptoms and prognosis. Rapid neurological decline with a fa...

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Detalles Bibliográficos
Autores principales: Ciammola, Andrea, Sangalli, Davide, Sassone, Jenny, Poletti, Barbara, Carelli, Laura, Banfi, Paolo, Pappacoda, Gabriele, Ceccherini, Isabella, Grossi, Alice, Maderna, Luca, Pingue, Monica, Girotti, Floriano, Silani, Vincenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851058/
https://www.ncbi.nlm.nih.gov/pubmed/31781017
http://dx.doi.org/10.3389/fneur.2019.01124

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851058/
https://www.ncbi.nlm.nih.gov/pubmed/31781017
http://dx.doi.org/10.3389/fneur.2019.01124

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