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Year | Number of Results |
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2012 | 1 |
2015 | 1 |
2017 | 1 |
2019 | 1 |
2024 | 0 |
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Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.
Ann Neurol. 2015 Sep;78(3):487-98. doi: 10.1002/ana.24466. Epub 2015 Jul 28.
Ann Neurol. 2015.
PMID: 26101835
Free PMC article.
Quantitative analysis of focused a-to-I RNA editing sites by ultra-high-throughput sequencing in psychiatric disorders.
Zhu H, Urban DJ, Blashka J, McPheeters MT, Kroeze WK, Mieczkowski P, Overholser JC, Jurjus GJ, Dieter L, Mahajan GJ, Rajkowska G, Wang Z, Sullivan PF, Stockmeier CA, Roth BL.
Zhu H, et al.
PLoS One. 2012;7(8):e43227. doi: 10.1371/journal.pone.0043227. Epub 2012 Aug 17.
PLoS One. 2012.
PMID: 22912834
Free PMC article.
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Pierpont syndrome associated with the p.Tyr446Cys missense mutation in TBL1XR1.
Slavotinek A, Pua H, Hodoglugil U, Abadie J, Shieh J, Van Ziffle J, Kvale M, Lee H, Kwok PY, Risch N, Sabbadini M.
Slavotinek A, et al.
Eur J Med Genet. 2017 Oct;60(10):504-508. doi: 10.1016/j.ejmg.2017.07.003. Epub 2017 Jul 4.
Eur J Med Genet. 2017.
PMID: 28687524
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Mutation Analysis of the Genes Linked to Early Onset Alzheimer's Disease and Frontotemporal Lobar Degeneration.
Luukkainen L, Helisalmi S, Kytövuori L, Ahmasalo R, Solje E, Haapasalo A, Hiltunen M, Remes AM, Krüger J.
Luukkainen L, et al.
J Alzheimers Dis. 2019;69(3):775-782. doi: 10.3233/JAD-181256.
J Alzheimers Dis. 2019.
PMID: 31127772
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