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    Case Report: A Novel Compound Heterozygote Mutation of the SCNN1B Gene Identified in a Chinese Familial Pseudohypoaldosteronism Disease Type I With Persistent Hyperkalemia

    Case Report: A Novel Compound Heterozygote Mutation of the SCNN1B Gene Identified in a Chinese Familial Pseudohypoaldosteronism Disease Type I With Persistent Hyperkalemia by Zongzhi Liu, Zongzhi Liu, Xiaojiao Wang, Zilong Zhang, Zixin Yang, Junyun Wang, Yajuan Wang

    Published 2022
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