The detection of GRN mutation carriers by progranulin blood protein levels from finger‐stick collect...
The detection of GRN mutation carriers by progranulin blood protein levels from finger‐stick collection
About this item
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Publisher
United States: John Wiley and Sons Inc
Journal title
Language
English
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Publisher
United States: John Wiley and Sons Inc
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INTRODUCTION
Heterozygous mutations in the progranulin gene (GRN) leading to decreased progranulin levels are one of the most frequent causes of inherited frontotemporal dementia (FTD). We evaluated progranulin levels in dried blood spots from capillary finger‐stick collection (DBScapillary).
METHODS
Paired venous Ethylenediaminetetraaceti...
Alternative Titles
Full title
The detection of GRN mutation carriers by progranulin blood protein levels from finger‐stick collection
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Record Identifier
TN_cdi_swepub_primary_oai_gup_ub_gu_se_344765
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_gup_ub_gu_se_344765
Other Identifiers
ISSN
1552-5260,1552-5279
E-ISSN
1552-5279
DOI
10.1002/alz.14259
