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Truncating mutations of HIBCH tend to cause severe phenotypes in cases with HIBCH deficiency: a case report and brief literature review

Crossref DOI link: https://doi.org/10.1038/s10038-018-0461-8

Published Online: 2018-04-27

Published Print: 2018-07

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

Authors

Tan, Hu

Chen, Xin

Lv, Weigang

Linpeng, Siyuan

Liang, Desheng

Wu, Lingqian
License Information

Text and Data Mining valid from 2018-04-27
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Article History

Received: 8 February 2018

Revised: 9 March 2018

Accepted: 31 March 2018

First Online: 27 April 2018

Compliance with ethical standards

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