- A Voxel Based Morphometric Analysis of Longitudinal Cortical Gray Matter Changes in Progranulin Mutation Carriers At-Risk for Frontotemporal Dementia: Preliminary Study
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Youn YC, Hsiung GY
- KMID: 2442934
- Dement Neurocogn Disord.
- 2015 Dec;14(4):163-167.
- doi: 10.12779/dnd.2015.14.4.163
BACKGROUND AND PURPOSE: One of the most common genetic causes of frontotemporal dementia (FTD) is mutation in the progranulin (PGRN) gene. The aim of this study is to assess the... -
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