Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

Two functionally related genes, FOXP2 and CNTNAP2, influence language abilities in families with rare syndromic and common nonsyndromic forms of impaired language, respectively. We investigated whether these genes are associated with component phenotypes of dyslexia and measures of sequential motor...

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Detalles Bibliográficos
Autores principales: Peter, Beate, Raskind, Wendy H., Matsushita, Mark, Lisowski, Mark, Vu, Tiffany, Berninger, Virginia W., Wijsman, Ellen M., Brkanac, Zoran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2010
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163991/
https://www.ncbi.nlm.nih.gov/pubmed/21484596
http://dx.doi.org/10.1007/s11689-010-9065-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163991/
https://www.ncbi.nlm.nih.gov/pubmed/21484596
http://dx.doi.org/10.1007/s11689-010-9065-0

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