Article
Clinical heterogeneity of the C9orf72 genetic mutation in frontotemporal dementia.
Neurocase - 1 Jan 2015
Devenney E, Foxe D, Dobson-Stone C, Kwok J B, Kiernan M C, Hodges J R
Abstract excerpt
The C9orf72 genetic mutation represents the most common cause of familial frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). Studies over the last 2 years have revealed a number of key features of this mutation in the fields of clinical neurology, imaging, pathology, and genetics. Despite these efforts, the clinical phenotype appears to extend beyond FTD and ALS into the realm of psychiatric...
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