Journal of Human Genetics (2015) 60, 165 & 2015 The Japan Society of Human Genetics All rights reserved 1434-5161/15 www.nature.com/jhg

CORRIGENDUM

Exome sequencing identifies a de novo mutation in HDAC8 associated with Cornelia de Lange syndrome Lei Feng, Daizhan Zhou, Zhou Zhang, Yun Liu and Yabo Yang Journal of Human Genetics (2015) 60, 165; doi:10.1038/jhg.2014.113 Correction to: Journal of Human Genetics 2014; 59, 536–539; doi:10.1038/jhg.2014.60; published online 7 August 2014 Since the publication of this article, the authors of the above paper have noticed an error in the description of mutation. The de novo

mutation ‘c.586A4T; p.M196K’ should have been ‘c.587A4T; p.M196K’. The authors apologize for any inconvenience caused.

Exome sequencing identifies a de novo mutation in HDAC8 associated with Cornelia de Lange syndrome.

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