Case Report: A Novel Compound Heterozygote Mutation of the？SCNN1B？Gene Identified in a Chinese Familial Pseudohypoaldosteronism Disease Type I With Persistent Hyperkalemia
| Authors： | Zongzhi Liu,？1 ,？2 ,？？？Xiaojiao Wang,？3 ,？？？Zilong Zhang,？4？Zixin Yang,？3？Junyun Wang,？5 ,？*？and？Yajuan Wang |
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| PubYear： | 2022 |
| Journal： | Front Pediatr |
