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1 Ergebnisse
1
Case Report: A Novel Compound Heterozygote Mutation of the ..:
Liu, Zongzhi
;
Wang, Xiaojiao
;
Zhang, Zilong
...
Frontiers in Pediatrics. 10 (2022) - p. , 2022
Link:
https://doi.org/10.3389/fped.2022.831284
RT Journal T1
Case Report: A Novel Compound Heterozygote Mutation of the SCNN1B Gene Identified in a Chinese Familial Pseudohypoaldosteronism Disease Type I With Persistent Hyperkalemia
UL https://suche.suub.uni-bremen.de/peid=cr-10.3389_fped.2022.831284&Exemplar=1&LAN=DE A1 Liu, Zongzhi A1 Wang, Xiaojiao A1 Zhang, Zilong A1 Yang, Zixin A1 Wang, Junyun A1 Wang, Yajuan PB Frontiers Media SA YR 2022 SN 2296-2360 JF Frontiers in Pediatrics VO 10 LK http://dx.doi.org/https://doi.org/10.3389/fped.2022.831284 DO https://doi.org/10.3389/fped.2022.831284 SF ELIB - SuUB Bremen
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