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Novel compound heterozygous mutations in SERPINH1 cause rare autosomal recessive osteogenesis imperfecta type X

Crossref DOI link: https://doi.org/10.1007/s00198-018-4448-2

Published Online: 2018-03-09

Published Print: 2018-06

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

Authors

Song, Y.

Zhao, D.

Xu, X.

Lv, F.

Li, L.

Jiang, Y.

Wang, O.

Xia, W.

Xing, X.

Li, M.
Funding

Funding for this research was provided by:

National Natural Science Foundation of China (81570802)

CAMS Initiative for Innovative Medicine (2016-I2M-3-003)

National Key Research and Development Program of China (2016YFC0901501)
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Article History

Received: 30 November 2017

Accepted: 13 February 2018

First Online: 9 March 2018

Compliance with ethical standards

: The study protocol was approved by the Scientific Research Ethics Committee of PUMCH, and the parents of the patient signed informed consent before they participated in this study.

: None.