Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC

Eleven loci with prior evidence for association with reading and language phenotypes were sequenced in 96 unrelated subjects with significant impairment in reading performance drawn from the Colorado Learning Disability Research Center collection. Out of 148 total individual missense variants identi...

Descripción completa

Detalles Bibliográficos
Autores principales: Adams, Andrew K., Smith, Shelley D., Truong, Dongnhu T., Willcutt, Erik G., Olson, Richard K., DeFries, John C., Pennington, Bruce F., Gruen, Jeffrey R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702371/
https://www.ncbi.nlm.nih.gov/pubmed/28866788
http://dx.doi.org/10.1007/s00439-017-1838-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702371/
https://www.ncbi.nlm.nih.gov/pubmed/28866788
http://dx.doi.org/10.1007/s00439-017-1838-z

Ejemplares similares