Splice Site, Frameshift and Chimeric GFAP Mutations in Alexander Disease

Alexander disease (AxD) is a usually fatal astrogliopathy primarily caused by mutations in the gene encoding GFAP, an intermediate filament protein expressed in astrocytes. We describe three patients with unique characteristics, and whose mutations have implications for AxD diagnosis and studies of...

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Detalhes bibliográficos
Main Authors: Flint, Daniel, Li, Rong, Webster, Lital S., Naidu, Sakkubai, Kolodny, Edwin, Percy, Alan, van der Knaap, Marjo, Powers, James M., Mantovani, John F., Ekstein, Josef, Goldman, James E., Messing, Albee, Brenner, Michael
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3674965/
https://ncbi.nlm.nih.gov/pubmed/22488673
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.22094
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