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 (in ALS). Methods In total, 36 non-symptomatic mutation carriers from ALS or FTD families were…

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