A case of familial frontotemporal dementia caused by a progranulin gene mutation

After Alzheimer’s disease, Frontotemporal dementia (FTD) is the most common cause of early-onset dementia. Several genetic mutations have been identified in familial FTD, with mutations in progranulin (GRN) accounting for approximately 20–25% of familial FTD cases and about 10% of total FTD cases. W...

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Bibliographic Details

Main Authors:	Lauryn Currens, Nigel Harrison, Maria Schmidt, Halima Amjad, Weiyi Mu, Sonja W. Scholz, Jee Bang, Alexander Pantelyat
Format:	Artigo
Language:	Inglês
Published:	Elsevier 2023-01-01
Series:	Clinical Parkinsonism & Related Disorders
Subjects:	Frontotemporal dementia FTD Progranulin, GRN Phenotypic heterogeneity
Online Access:	http://www.sciencedirect.com/science/article/pii/S2590112523000312
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