A commentary on exome sequencing identifies a de novo mutation in HDAC8 associated with Cornelia de Lange syndrome
Crossref DOI link: https://doi.org/10.1038/jhg.2014.68
Published Online: 2014-08-07
Published Print: 2014-09
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Sun, Liangdan
Text and Data Mining valid from 2014-08-07
Article History
First Online: 7 August 2014