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Authors
Kong, Xinxin
Boeckhaus, Jan
Wang, Fang
Shi, Chunyan
Zhang, Hongwen
Gross, Oliver
Ding, Jie
Zhang, Yanqin
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Funding
Funding for this research was provided by:
National Science and Technology Major Project (2022ZD0116003)
Beijing key laboratory of molecular diagnosis and study on pediatric genetic diseases (BZ0317)
DFG SINO-GERMAN MOBILITY PROGRAMME (M0166)
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Article History
Received: 7 June 2024
Accepted: 14 February 2025
First Online: 20 May 2025
Declarations
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: No conflicts of interest are declared by the authors.
: This observational, retrospective study was conducted in accordance with the declaration of Helsinki. Data acquisition in China was reviewed and approved by the Institutional Review Board of Peking University First Hospital (2022 [051] V1.0). Informed consent for this study was obtained from all patients. Data acquisition in Europe was part of the European Alport registry, which has been reviewed and approved by the Institutional Review Board of University Medicine Goettingen (AZ 10/11/06).
: All procedures were approved by the Peking University First Hospital Institutional Review Board (2022 [051] V1.0) and the University Medicine Goettingen Institutional Review Board (AZ 10/11/06).
: Informed consent was obtained from all individual participants.
