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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

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