A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2 The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters. Citation Fedorenko, Evelina et al. “A Highly Penetrant Form of Childhood Apraxia of Speech Due to Deletion of 16p11.2.” European Journal of Human Genetics 24, 2 (July 2015): 302–306 © 2016 Macmillan Publishers Limited As Published https://doi.org/10.1038/ejhg.2015.149 Publisher Nature Publishing Group Version Author's final manuscript Citable link http://hdl.handle.net/1721.1/113018 Terms of Use Creative Commons Attribution-Noncommercial-Share Alike Detailed Terms http://creativecommons.org/licenses/by-nc-sa/4.0/ A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2 Authors: Evelina Fedorenko1^, Angela Morgan2^, Elizabeth Murray2, Annie Cardinaux3, Cristina Mei2, Helen Tager-Flusberg4, Simon E. Fisher5,6, Nancy Kanwisher3,7 1Massachusetts General Hospital, Department of Psychiatry (Boston, MA); 2Murdoch Childrens Research Institute (Melbourne, Australia); 3Massachusetts Institute of Technology, Brain and Cognitive Sciences Department (Cambridge, MA); 4Boston University, Department of Psychological and Brain Sciences (Boston, MA); 5Max Planck Institute for Psycholinguistics (Nijmegen, Netherlands); 6Donders Institute for Brain, Cognition and Behaviour (Nijmegen, Netherlands); 7McGovern Institute for Brain Research (Cambridge, MA) ^ These authors contributed equally to this manuscript. Running title: Speech apraxia in children with 16p11.2 Corresponding author: Professor Evelina Fedorenko Psychiatry Department Massachusetts General Hospital Building 149, East 13th St Charlestown, MA 02129 Email:
[email protected]. Phone: 1-617-417-5044 1 Summary Individuals with heterozygous 16p11.2 deletions reportedly suffer from a variety of difficulties with speech and language.