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A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.
Nat Genet. 2015 Jan;47(1):39-46. doi: 10.1038/ng.3144. Epub 2014 Nov 17.
Nat Genet. 2015.
PMID: 25401298
Free PMC article.
BAP1 Germline Mutations in Finnish Patients with Uveal Melanoma.
Turunen JA, Markkinen S, Wilska R, Saarinen S, Raivio V, Täll M, Lehesjoki AE, Kivelä TT.
Turunen JA, et al. Among authors: markkinen s.
Ophthalmology. 2016 May;123(5):1112-7. doi: 10.1016/j.ophtha.2016.01.008. Epub 2016 Feb 12.
Ophthalmology. 2016.
PMID: 26876698
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Population-based analysis of BAP1 germline variations in patients with uveal melanoma.
Repo P, Järvinen RS, Jäntti JE, Markkinen S, Täll M, Raivio V, Turunen JA, Kivelä TT.
Repo P, et al. Among authors: markkinen s.
Hum Mol Genet. 2019 Jul 15;28(14):2415-2426. doi: 10.1093/hmg/ddz076.
Hum Mol Genet. 2019.
PMID: 31058963
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Mismatches in Gene Deletions and Kidney-related Proteins as Candidates for Histocompatibility Factors in Kidney Transplantation.
Markkinen S, Helanterä I, Lauronen J, Lempinen M, Partanen J, Hyvärinen K.
Markkinen S, et al.
Kidney Int Rep. 2022 Sep 6;7(11):2484-2494. doi: 10.1016/j.ekir.2022.08.032. eCollection 2022 Nov.
Kidney Int Rep. 2022.
PMID: 36531875
Free PMC article.
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