Journal article
A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2
E Fedorenko, A Morgan, E Murray, A Cardinaux, C Mei, H Tager-Flusberg, SE Fisher, N Kanwisher
European Journal of Human Genetics | NATURE PUBLISHING GROUP | Published : 2016
Abstract
Correction to: European Journal of Human Genetics advance online publication, 15 July 2015; doi:10.1038/ejhg.2015.149 Dr Simon E Fisher’s affiliation unfortunately contained an error. This has been corrected in the online version and the print version, which also appears in this issue.