Rare GRN mutation in a patient diagnosed with primary progressive aphasia and parkinsonism
- 18 August 2022
- journal article
- letter
- Published by Springer Nature in Acta Neurologica Belgica
- Vol. 123 (2) , 727-729
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- GRN mutation in a patient with a behavioral variant of frontotemporal lobar degeneration (bvFTD)Folia Neuropathologica, 2017
- Frontotemporal dementiaThe Lancet, 2015
- Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadicsBrain, 2012
- Classification of primary progressive aphasia and its variantsNeurology, 2011
- Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementiaHuman Mutation, 2008
- Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Nature, 2006
- Cellular Localization of Gene Expression for ProgranulinJournal of Histochemistry & Cytochemistry, 2000