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Whole exome sequencing reveals a stop-gain mutation of PKD2 in an autosomal dominant polycystic kidney disease family complicated with aortic dissection

Crossref DOI link: https://doi.org/10.1186/s12881-018-0536-6

Published Online: 2018-01-30

Published Print: 2018-12

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

Authors

Zhang, Wenwen

Han, Qian

Liu, Zhao

Zhou, Wei

Cao, Qing

Zhou, Weimin https://orcid.org/0000-0003-1265-4522
Funding

Funding for this research was provided by:

National Natural Science Foundation of China (81660086)
More Information

Article History

Received: 19 March 2017

Accepted: 24 January 2018

First Online: 30 January 2018

Ethics approval and consent to participate

: Ethical approval was obtained from the institutional review board, The Second Affiliated Hospital of Nanchang University. After explanation of the possible consequences of the study, written informed consent was obtained from all study participants.

: Consent for publication of the case was obtained for each participant, including case description, clinical data and images.

: The authors declare that they have no competing interest.

: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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