Mutations in multidomain protein MEGF8 identify a carpenter syndrome subtype associated with defective lateralization

Stephen R F Twigg, Deborah Lloyd, Dagan Jenkins, Nursel E. Elçioglu, Christopher D O Cooper, Nouriya Al-Sannaa, Ali Annagür, Gabriele Gillessen-Kaesbach, Irina Hüning, Samantha J L Knight, Judith A. Goodship, Bernard D. Keavney, Philip L. Beales, Opher Gileadi, Simon J. McGowan, Andrew O M Wilkie^*

^*Corresponding author for this work