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Whole-exome sequencing in children with dyslexia identifies rare variants in CLDN3 and ion channel genes
Krzysztof Marianski, Joel B. Talcott, John Stein, Anthony P. Monaco, Simon E. Fisher, Dorothy V.M. Bishop, Dianne F. Newbury, Silvia Paracchini*
*Corresponding author for this work
Research output: Working paper › Preprint