Exome sequencing identifies a de novo mutation in HDAC8 associated with Cornelia de Lange syndrome (vol 60, pg 164, 2015)

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.586A>T; p.M196K’ should have been‘c.