Type II (adult onset) Alexander disease in a paraplegic male with a rare D128N mutation in the GFAP gene

Abstract not available.

Detalles Bibliográficos
Autores principales: Chang, Ki-Eun, Pratt, Drew, Mishra, Bibhuti B., Edwards, Nancy, Hallett, Mark, Ray-Chaudhury, Abhik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dustri-Verlag Dr. Karl Feistle 2015
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766795/
https://www.ncbi.nlm.nih.gov/pubmed/25997626
http://dx.doi.org/10.5414/NP300863

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766795/
https://www.ncbi.nlm.nih.gov/pubmed/25997626
http://dx.doi.org/10.5414/NP300863

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