Zhang, Yanqin
Böckhaus, Jan
Wang, Fang
Wang, Suxia
Rubel, Diana
Gross, Oliver
Ding, Jie
Funding for this research was provided by:
National Key Research and Development Program of China (No. 2016YFC0901505)
Beijing key laboratory of molecular diagnosis and study on pediatric genetic diseases (BZ0317)
German Research Foundation DFG (GR 1852/6-1 to OG)
German Federal Ministry of Education and Research (01KG1104 to OG)
European Alport Registry is supported by the Association pour l’Information et la Recherche sur les Maladies Rénales Génétiques (AIRG-France)
K. C. Wong Education Foundation and DAAD
Article History
Received: 21 September 2020
Revised: 20 February 2021
Accepted: 2 March 2021
First Online: 27 March 2021
Declarations
:
: The authors declare that they have no conflict of interest.