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Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers—a developmental disorder

BACKGROUND: A mutation in C9orf72 constitute a cross-link between amyotrophic lateral sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient groups may present with either cognitive impairment of predominantly behaviour or language (in FTD) or motor dysfunctions...

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Detalles Bibliográficos
Autores principales:	Lulé, Dorothée E, Müller, Hans-Peter, Finsel, Julia, Weydt, Patrick, Knehr, Antje, Winroth, Ivar, Andersen, Peter, Weishaupt, Jochen, Uttner, Ingo, Kassubek, Jan, Ludolph, Albert C
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BMJ Publishing Group 2020
Materias:	Cognitive Neurology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569387/ https://www.ncbi.nlm.nih.gov/pubmed/32855285 http://dx.doi.org/10.1136/jnnp-2020-323671

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