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EAST/SeSAME syndrome: Review of the literature and introduction of four new Latvian patients.
Clin Genet. 2019 Jan;95(1):63-78. doi: 10.1111/cge.13374. Epub 2018 Jul 8.
Clin Genet. 2019.
PMID: 29722015
Review.
Complete mtDNA sequencing reveals mutations m.9185T>C and m.13513G>A in three patients with Leigh syndrome.
Pelnena D, Burnyte B, Jankevics E, Lace B, Dagyte E, Grigalioniene K, Utkus A, Krumina Z, Rozentale J, Adomaitiene I, Stavusis J, Pliss L, Inashkina I.
Pelnena D, et al.
Mitochondrial DNA A DNA Mapp Seq Anal. 2018 Oct;29(7):1115-1120. doi: 10.1080/24701394.2017.1413365. Epub 2017 Dec 12.
Mitochondrial DNA A DNA Mapp Seq Anal. 2018.
PMID: 29228836
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A New Baltic Population-Specific Human Genetic Marker in the PMCA4 Gene.
Stavusis J, Inashkina I, Lace B, Pelnena D, Limborska S, Khrunin A, Kucinskas V, Krumina A, Piekuse L, Zorn B, Fodina V, Punab M, Erenpreiss J.
Stavusis J, et al. Among authors: pelnena d.
Hum Hered. 2016;82(3-4):140-146. doi: 10.1159/000481434. Epub 2017 Nov 2.
Hum Hered. 2016.
PMID: 29131013
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Effects of a Mutation in the HSPE1 Gene Encoding the Mitochondrial Co-chaperonin HSP10 and Its Potential Association with a Neurological and Developmental Disorder.
Bie AS, Fernandez-Guerra P, Birkler RI, Nisemblat S, Pelnena D, Lu X, Deignan JL, Lee H, Dorrani N, Corydon TJ, Palmfeldt J, Bivina L, Azem A, Herman K, Bross P.
Bie AS, et al. Among authors: pelnena d.
Front Mol Biosci. 2016 Oct 7;3:65. doi: 10.3389/fmolb.2016.00065. eCollection 2016.
Front Mol Biosci. 2016.
PMID: 27774450
Free PMC article.
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