Associated Papers
Screening for MAPT and PGRN mutations in Korean patients with PSP/CBS/FTD.
Kim HJ et al.
Parkinsonism & Related Disorders, 2010
Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update.
Gijselinck I et al.
Human Mutation, 2008
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.
van der Zee J et al.
Human Mutation, 2007
PGRN mutations in northern Italy.
Borroni B et al.
Alzheimer Disease and Associated Disorders, 0
Higher than expected progranulin mutation rate in a case series of Italian FTLD patients.
Tremolizzo L et al.
Alzheimer Disease and Associated Disorders, 0
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