Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. by Pagnamenta, A, Bacchelli, E, de Jonge, M, Mirza, G, Scerri, T, Minopoli, F, Chiocchetti, A, Ludwig, K, Hoffmann, P, Paracchini, S, Lowy, E, Harold, D, Chapman, J, Klauck, S, Poustka, F, Houben, R, Staal, W, Ophoff, R, O'Donovan, M, Williams, J, Nöthen, M, Schulte-Körne, G, Deloukas, P, Ragoussis, J, Bailey, A