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Complete loss of function of the ubiquitin ligase HERC2 causes a severe neurodevelopmental phenotype

Crossref DOI link: https://doi.org/10.1038/ejhg.2016.139

Published Online: 2016-10-19

Published Print: 2017-01

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Morice-Picard, Fanny

Benard, Giovanni

Rezvani, Hamid R

Lasseaux, Eulalie

Simon, Delphine

Moutton, Sébastien

Rooryck, Caroline

Lacombe, Didier

Baumann, Clarisse

Arveiler, Benoit https://orcid.org/0000-0002-2987-2932
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Text and Data Mining valid from 2016-10-19
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Article History

Received: 29 March 2016

Revised: 28 August 2016

Accepted: 13 September 2016

First Online: 19 October 2016

Competing interests

: The authors declare no conflict of interest.