GRN 3′UTR+78 C>T is not associated with risk for Parkinson's disease

9Citations
Citations of this article
33Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Background and purpose: A single nucleotide polymorphism in the 3′-untranslated region of the progranulin gene (GRN; 3′UTR+78C>T; rs5848) was reported to alter the risk for frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U). rs5848 is located within a micro-RNA binding site and affects the expression of GRN. Methods: As FTLD-U patients often present with parkinsonism, we investigated the association of GRN rs5848 and risk of Parkinson's disease in two Caucasian patient-control series (n = 1413) from the US and Poland. Results: No association was observed between rs5848 and susceptibility to Parkinson's disease (individual series and combined analysis). Conclusions: This finding shows that GRN rs5848 does not affect the risk of Parkinson's disease in the US and Polish populations. © 2009 EFNS.

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Jasinska-Myga, B., Wider, C., Opala, G., Krygowska-Wajs, A., Barcikowska, M., Czyzewski, K., … Wszolek, Z. K. (2009). GRN 3′UTR+78 C>T is not associated with risk for Parkinson’s disease. European Journal of Neurology, 16(8), 909–911. https://doi.org/10.1111/j.1468-1331.2009.02621.x

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 14

56%

Professor / Associate Prof. 7

28%

Researcher 4

16%

Readers' Discipline

Tooltip

Neuroscience 11

46%

Agricultural and Biological Sciences 6

25%

Medicine and Dentistry 4

17%

Psychology 3

13%

Save time finding and organizing research with Mendeley

Sign up for free