No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration.

doi:10.1016/j.neurobiolaging.2009.04.009

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Article

No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration.

Neurobiology of aging - 1 Apr 2011

Rollinson Sara, Rohrer Jonathan D, van der Zee Julie, Sleegers Kristel, Mead Simon, Engelborghs Sebastiaan, Collinge John, De Deyn Peter P, Mann David M A, Van Broeckhoven Christine, Pickering-Brown Stuart M

Abstract excerpt

Frontotemporal lobar degeneration (FTLD) is a highly familial neurodegenerative disease. It has been claimed that homozygosity of the SNP rs5848 located in the 3'UTR of progranulin increases risk for FTLD. We have attempted to replicate the association of rs5848 in three independent FTLD cohorts....

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PMID: 19446372
DOI: 10.1016/j.neurobiolaging.2009.04.009

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19446372-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration.PMID 19446372Read ↗

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