Imaging genetics of FOXP2 in dyslexia

Dyslexia is a developmental disorder characterised by extensive difficulties in the acquisition of reading or spelling. Genetic influence is estimated at 50–70%. However, the link between genetic variants and phenotypic deficits is largely unknown. Our aim was to investigate a role of genetic varian...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Wilcke, Arndt, Ligges, Carolin, Burkhardt, Jana, Alexander, Michael, Wolf, Christiane, Quente, Elfi, Ahnert, Peter, Hoffmann, Per, Becker, Albert, Müller-Myhsok, Bertram, Cichon, Sven, Boltze, Johannes, Kirsten, Holger
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2012
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3260915/
https://ncbi.nlm.nih.gov/pubmed/21897444
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2011.160
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados