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A polymorphism in intronic sequence affects the processing of MAO-B gene in patients with Parkinson disease” [FEBS Lett. 586 (2012) 3698–3704]
FEBS Letters 587 (2013) 302–303
journal homepage: www.FEBSLetters.org
Corrigendum
Corrigendum to ‘‘G/A polymorphism in intronic sequence affects the processing of MAO-B gene in patients with Parkinson disease’’ [FEBS Lett. 586 (2012) 3698–3704] Egle Jakubauskiene a, Valda Janaviciute a, Inga Peciuliene a, Peter Söderkvist b, Arvydas Kanopka a,⇑ a b
Department of Immunology and Cell Biology, Vilnius University, Institute of Biotechnology, LT-02241 Vilnius, Lithuania Department of Clinical and Experimental Medicine, Division of Cell Biology, Linköping University, SE-581 85 Linköping, Sweden
The Supplementary material was missing. The manuscript includes two Supplementary figures as follows:
Fig. S1. MAO-B gene intron 13 regions isolated from platelets of healthy individuals (a) and patients with Parkinson disease (b) sequencing data. Reverse primer P4 was used for sequencing.
DOI of original article: http://dx.doi.org/10.1016/j.febslet.2012.08.028
⇑ Corresponding author. Fax: +370 5 2602116. E-mail address: [email protected] (A. Kanopka).
0014-5793/$36.00 Ó 2012 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies. http://dx.doi.org/10.1016/j.febslet.2012.12.001
E. Jakubauskiene et al. / FEBS Letters 587 (2013) 302–303
303
Fig. S2. Branch point determination of MaoBg transcript (a) and MaoBa pre-mRNA (b) using bioinformatics approach. The data shows that about 85% probability that branch point is within sequence...TGGATATCTCCAA (branch point is A in bold). Possible branch points are indicated by arrow. Dimorphism sites are indicated by asterisk.
journal homepage: www.FEBSLetters.org
Corrigendum
Corrigendum to ‘‘G/A polymorphism in intronic sequence affects the processing of MAO-B gene in patients with Parkinson disease’’ [FEBS Lett. 586 (2012) 3698–3704] Egle Jakubauskiene a, Valda Janaviciute a, Inga Peciuliene a, Peter Söderkvist b, Arvydas Kanopka a,⇑ a b
Department of Immunology and Cell Biology, Vilnius University, Institute of Biotechnology, LT-02241 Vilnius, Lithuania Department of Clinical and Experimental Medicine, Division of Cell Biology, Linköping University, SE-581 85 Linköping, Sweden
The Supplementary material was missing. The manuscript includes two Supplementary figures as follows:
Fig. S1. MAO-B gene intron 13 regions isolated from platelets of healthy individuals (a) and patients with Parkinson disease (b) sequencing data. Reverse primer P4 was used for sequencing.
DOI of original article: http://dx.doi.org/10.1016/j.febslet.2012.08.028
⇑ Corresponding author. Fax: +370 5 2602116. E-mail address: [email protected] (A. Kanopka).
0014-5793/$36.00 Ó 2012 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies. http://dx.doi.org/10.1016/j.febslet.2012.12.001
E. Jakubauskiene et al. / FEBS Letters 587 (2013) 302–303
303
Fig. S2. Branch point determination of MaoBg transcript (a) and MaoBa pre-mRNA (b) using bioinformatics approach. The data shows that about 85% probability that branch point is within sequence...TGGATATCTCCAA (branch point is A in bold). Possible branch points are indicated by arrow. Dimorphism sites are indicated by asterisk.