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European Journal of Human Genetics logoLink to European Journal of Human Genetics
. 2016 Jan 14;24(2):310. doi: 10.1038/ejhg.2015.230

A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2

Evelina Fedorenko, Angela Morgan, Elizabeth Murray, Annie Cardinaux, Cristina Mei, Helen Tager-Flusberg, Simon E Fisher, Nancy Kanwisher
PMCID: PMC4717201  PMID: 26763793

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.


Articles from European Journal of Human Genetics are provided here courtesy of Nature Publishing Group

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