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. 2017 Apr 26;7:1172. doi: 10.1038/s41598-017-01178-5

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Detection of AKAP7 splice variants in peripheral blood. (A) Exon maps of previously validated (blue) and bioinformatically predicted (grey) AKAP7 splice variants with the location of microarray probes and variant-specific priming sites. PEX denotes a bioinformatically predicted exon. (B) AKAP7 splice variant-specific RT-PCR products amplified from peripheral blood-derived cDNA obtained from two non-stroke donors and two stroke patients.