Corrigendum | Published:

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

Journal of Human Genetics volume 60, page 165 (2015) | Download Citation


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.587A>T; p.M196K’.

The authors apologize for any inconvenience caused.

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