White matter lesions in FTLD: distinct phenotypes characterize GRN and C9ORF72 mutations

Detalles Bibliográficos
Autores principales: Ameur, Fatima, Colliot, Olivier, Caroppo, Paola, Ströer, Sebastian, Dormont, Didier, Brice, Alexis, Azuar, Carole, Dubois, Bruno, Le Ber, Isabelle, Bertrand, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2016
Materias:
Clinical/Scientific Notes
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817905/
https://www.ncbi.nlm.nih.gov/pubmed/27066584
http://dx.doi.org/10.1212/NXG.0000000000000047

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817905/
https://www.ncbi.nlm.nih.gov/pubmed/27066584
http://dx.doi.org/10.1212/NXG.0000000000000047

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