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A novel MAP3K7 splice mutation causes cardiospondylocarpofacial syndrome with features of hereditary connective tissue disorder

Crossref DOI link: https://doi.org/10.1038/s41431-017-0079-x

Published Online: 2018-02-21

Published Print: 2018-04

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

Authors

Morlino, Silvia

Castori, Marco

Dordoni, Chiara

Cinquina, Valeria

Santoro, Graziano

Grammatico, Paola

Venturini, Marina

Colombi, Marina

Ritelli, Marco
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Article History

Received: 7 June 2017

Revised: 28 November 2017

Accepted: 5 December 2017

First Online: 21 February 2018

Compliance with ethical standards

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: The authors declare that they have no conflict of interest.