A1 Journal article (refereed)
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia (2015)

Matsson, H., Huss, M., Persson, H., Einarsdottir, E., Tiraboschi, E., Nopola-Hemmi, J., Schumacher, J., Neuhoff, N., Warnke, A., Lyytinen, H., Schulte-Körne, G., Nöthen, M. M., Leppänen, P. H., Peyrard-Janvid, M., & Kere, J. (2015). Polymorphisms in DCDC2 and S100B associate with developmental dyslexia. Journal of Human Genetics, 60(7), 399-401. https://doi.org/10.1038/jhg.2015.37

JYU authors or editors

Publication details

All authors or editors: Matsson, Hans; Huss, Mikael; Persson, Helena; Einarsdottir, Elisabet; Tiraboschi, Ettore; Nopola-Hemmi, Jaana; Schumacher, Johannes; Neuhoff, Nina; Warnke, Andreas; Lyytinen, Heikki; et al.

Journal or series: Journal of Human Genetics

ISSN: 1434-5161

eISSN: 1435-232X

Publication year: 2015

Volume: 60

Issue number: 7

Pages range: 399–401

Publisher: Nature Publishing Group; Japan Society of Human Genetics

Publication country: Japan

Publication language: English

DOI: https://doi.org/10.1038/jhg.2015.37

Publication open access: Openly available

Publication channel open access: Partially open access channel

Publication is parallel published (JYX): https://jyx.jyu.fi/handle/123456789/46611

Additional information: Short Communication.

Keywords: genetics

Free keywords: individual genotyping; single-nucleotide polymorphisms; developmental dyslexia

Contributing organizations

Ministry reporting: Yes

Reporting Year: 2015

JUFO rating: 1