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...

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Detalhes bibliográficos
Publicado no:Hum Genet
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2017
Assuntos:
Original Investigation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5702371/
https://ncbi.nlm.nih.gov/pubmed/28866788
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-017-1838-z
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