A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2
2016
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.
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