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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:J Hum Genet
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: Nature Publishing Group 2015
Ämnen:
Short Communication
Länkar: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
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk