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Year | Number of Results |
---|---|
2008 | 1 |
2010 | 1 |
2012 | 1 |
2015 | 1 |
2024 | 0 |
PubMed for id: 108903149
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Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese.
Neurobiol Aging. 2012 Aug;33(8):1843.e19-24. doi: 10.1016/j.neurobiolaging.2011.12.037. Epub 2012 Mar 7.
Neurobiol Aging. 2012.
PMID: 22402017
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.
Pottier C, Bieniek KF, Finch N, van de Vorst M, Baker M, Perkersen R, Brown P, Ravenscroft T, van Blitterswijk M, Nicholson AM, DeTure M, Knopman DS, Josephs KA, Parisi JE, Petersen RC, Boylan KB, Boeve BF, Graff-Radford NR, Veltman JA, Gilissen C, Murray ME, Dickson DW, Rademakers R.
Pottier C, et al.
Acta Neuropathol. 2015 Jul;130(1):77-92. doi: 10.1007/s00401-015-1436-x. Epub 2015 May 6.
Acta Neuropathol. 2015.
PMID: 25943890
Free PMC article.
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Mutations of optineurin in amyotrophic lateral sclerosis.
Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, Suzuki N, Aoki M, Kawata A, Hirai T, Kato T, Ogasawara K, Hirano A, Takumi T, Kusaka H, Hagiwara K, Kaji R, Kawakami H.
Maruyama H, et al.
Nature. 2010 May 13;465(7295):223-6. doi: 10.1038/nature08971. Epub 2010 Apr 28.
Nature. 2010.
PMID: 20428114
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Mechanisms for human genomic rearrangements.
Gu W, Zhang F, Lupski JR.
Gu W, et al.
Pathogenetics. 2008 Nov 3;1(1):4. doi: 10.1186/1755-8417-1-4.
Pathogenetics. 2008.
PMID: 19014668
Free PMC article.
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