Polymorphisms in DCDC2 and S100B associate with developmental dyslexia

Hans Matsson; Mikael Huss; Helena Persson; Elisabet Einarsdottir; Ettore Tiraboschi; Jaana Nopola-Hemmi; Johannes Schumacher; Nina Neuhoff; Andreas Warnke; Heikki Lyytinen; Gert Schulte-Korne; Markus M. Nothen; Paavo H. T. Leppanen; Myriam Peyrard-Janvid; Juha Kere

doi:10.1038/jhg.2015.37

Polymorphisms in DCDC2 and S100B associate with developmental dyslexia

Hans Matsson, Mikael Huss, Helena Persson, Elisabet Einarsdottir, Ettore Tiraboschi, Jaana Nopola-Hemmi, Johannes Schumacher, Nina Neuhoff, Andreas Warnke, Heikki Lyytinen, Gert Schulte-Korne, Markus M. Nothen, Paavo H. T. Leppanen, Myriam Peyrard-Janvid, Juha Kere

Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

Originalspråk	engelska
Tidskrift	Journal of Human Genetics
Volym	60
Nummer	7
Sidor (från-till)	399-401
Antal sidor	3
ISSN	1434-5161
DOI	https://doi.org/10.1038/jhg.2015.37
Status	Publicerad - juli 2015
MoE-publikationstyp	A1 Tidskriftsartikel-refererad

Vetenskapsgrenar

3111 Biomedicinska vetenskaper

Åtkomst av dokument

10.1038/jhg.2015.37

Citera det här

Matsson, H., Huss, M., Persson, H., Einarsdottir, E., Tiraboschi, E., Nopola-Hemmi, J., Schumacher, J., Neuhoff, N., Warnke, A., Lyytinen, H., Schulte-Korne, G., Nothen, M. M., Leppanen, P. H. T., 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

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title = "Polymorphisms in DCDC2 and S100B associate with developmental dyslexia",

keywords = "CANDIDATE GENES, MICRORNA, MUTATIONS, GENETICS, SITE, CELL, 3111 Biomedicine",

author = "Hans Matsson and Mikael Huss and Helena Persson and Elisabet Einarsdottir and Ettore Tiraboschi and Jaana Nopola-Hemmi and Johannes Schumacher and Nina Neuhoff and Andreas Warnke and Heikki Lyytinen and Gert Schulte-Korne and Nothen, {Markus M.} and Leppanen, {Paavo H. T.} and Myriam Peyrard-Janvid and Juha Kere",

year = "2015",

month = jul,

doi = "10.1038/jhg.2015.37",

language = "English",

volume = "60",

pages = "399--401",

journal = "Journal of Human Genetics",

issn = "1434-5161",

publisher = "Nature Publishing Group",

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Matsson, H, Huss, M, Persson, H, Einarsdottir, E, Tiraboschi, E, Nopola-Hemmi, J, Schumacher, J, Neuhoff, N, Warnke, A, Lyytinen, H, Schulte-Korne, G, Nothen, MM, Leppanen, PHT, Peyrard-Janvid, M & Kere, J 2015, 'Polymorphisms in DCDC2 and S100B associate with developmental dyslexia', Journal of Human Genetics, vol. 60, nr. 7, s. 399-401. https://doi.org/10.1038/jhg.2015.37

TY - JOUR

T1 - Polymorphisms in DCDC2 and S100B associate with developmental dyslexia

AU - Matsson, Hans

AU - Huss, Mikael

AU - Persson, Helena

AU - Einarsdottir, Elisabet

AU - Tiraboschi, Ettore

AU - Nopola-Hemmi, Jaana

AU - Schumacher, Johannes

AU - Neuhoff, Nina

AU - Warnke, Andreas

AU - Lyytinen, Heikki

AU - Schulte-Korne, Gert

AU - Nothen, Markus M.

AU - Leppanen, Paavo H. T.

AU - Peyrard-Janvid, Myriam

AU - Kere, Juha

PY - 2015/7

Y1 - 2015/7

KW - CANDIDATE GENES

KW - MICRORNA

KW - MUTATIONS

KW - GENETICS

KW - SITE

KW - CELL

KW - 3111 Biomedicine

U2 - 10.1038/jhg.2015.37

DO - 10.1038/jhg.2015.37

M3 - Article

SN - 1434-5161

VL - 60

SP - 399

EP - 401

JO - Journal of Human Genetics

JF - Journal of Human Genetics

IS - 7

ER -