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An inherited FGFR2 mutation increased osteogenesis gene expression and result in Crouzon syndrome

Crossref DOI link: https://doi.org/10.1186/s12881-018-0607-8

Published Online: 2018-05-30

Published Print: 2018-12

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

Authors

Fan, Jiayan

Li, Yinwei

Jia, Renbing

Fan, Xianqun http://orcid.org/0000-0001-7442-1391
Funding

Funding for this research was provided by:

The National Natural Science Foundation of China (81502481)

Foundation of Ninth People’s Hospital Affiliated to Shanghai JiaoTong University School of Medicine (2014A05)

the Science and Technology Commission of Shanghai (17DZ2260100)
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Article History

Received: 10 January 2018

Accepted: 18 May 2018

First Online: 30 May 2018

Ethics approval and consent to participate

: The research was carried out according to the principles of the Declaration of Helsinki; informed consent was obtained and Shanghai Ninth People’s Hospital Ethics Committee approved the study. A copy of the written consent is available for review by the Editor of this journal.

: Written informed consent was obtained from the patient for publication of this case report and any accompanying images.

: The authors declare that they have no competing interests.

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