학술논문

A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy.
Document Type
journal article
Source
Journal of Alzheimer's Disease; 2016, Vol. 53 Issue 2, p475-485, 11p
Subject
FRONTOTEMPORAL dementia
FRONTOTEMPORAL lobar degeneration
PROGRANULIN
GENETIC mutation
GENETIC testing
DIAGNOSIS
GENETICS
Language
ISSN
13872877
Abstract
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