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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Veröffentlicht in:Hum Genet
Hauptverfasser: Adams, Andrew K., Smith, Shelley D., Truong, Dongnhu T., Willcutt, Erik G., Olson, Richard K., DeFries, John C., Pennington, Bruce F., Gruen, Jeffrey R.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Springer Berlin Heidelberg 2017
Schlagworte:
Original Investigation
Online Zugang: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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