Polymorphisms in DCDC2 and S100B associate with developmental dyslexia

Genetic studies of complex traits have become increasingly successful as progress is made in next-generation sequencing. We aimed at discovering single nucleotide variation present in known and new candidate genes for developmental dyslexia: CYP19A1, DCDC2, DIP2A, DYX1C1, GCFC2 (also known as C2orf3...

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Veröffentlicht in:J Hum Genet
Hauptverfasser: Matsson, Hans, Huss, Mikael, Persson, Helena, Einarsdottir, Elisabet, Tiraboschi, Ettore, Nopola-Hemmi, Jaana, Schumacher, Johannes, Neuhoff, Nina, Warnke, Andreas, Lyytinen, Heikki, Schulte-Körne, Gert, Nöthen, Markus M, Leppänen, Paavo HT, Peyrard-Janvid, Myriam, Kere, Juha
Format: Artigo
Sprache:Inglês
Veröffentlicht: Nature Publishing Group 2015
Schlagworte:
Short Communication
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4521290/
https://ncbi.nlm.nih.gov/pubmed/25877001
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jhg.2015.37
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