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Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.
Nat Commun. 2015 Jun 16;6:7247. doi: 10.1038/ncomms8247.
Nat Commun. 2015.
PMID: 26077951
Free PMC article.
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.
Finch N, Carrasquillo MM, Baker M, Rutherford NJ, Coppola G, Dejesus-Hernandez M, Crook R, Hunter T, Ghidoni R, Benussi L, Crook J, Finger E, Hantanpaa KJ, Karydas AM, Sengdy P, Gonzalez J, Seeley WW, Johnson N, Beach TG, Mesulam M, Forloni G, Kertesz A, Knopman DS, Uitti R, White CL 3rd, Caselli R, Lippa C, Bigio EH, Wszolek ZK, Binetti G, Mackenzie IR, Miller BL, Boeve BF, Younkin SG, Dickson DW, Petersen RC, Graff-Radford NR, Geschwind DH, Rademakers R.
Finch N, et al.
Neurology. 2011 Feb 1;76(5):467-74. doi: 10.1212/WNL.0b013e31820a0e3b. Epub 2010 Dec 22.
Neurology. 2011.
PMID: 21178100
Free PMC article.
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Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulin.
McDade E, Boeve BF, Burrus TM, Boot BP, Kantarci K, Fields J, Lowe VJ, Peller P, Knopman D, Baker M, Finch N, Rademakers R, Petersen R.
McDade E, et al.
Neurology. 2012 Apr 17;78(16):1245-9. doi: 10.1212/WNL.0b013e318251594c. Epub 2012 Apr 4.
Neurology. 2012.
PMID: 22491866
Free PMC article.
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