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    Functional analysis of compound heterozygous variations in the CLCNKB gene in a patient with Bartter syndrome type Ⅲ

    Functional analysis of compound heterozygous variations in the CLCNKB gene in a patient with Bartter syndrome type Ⅲ oleh Yu-wen Cai, Xue-qin Cheng, Ruo-chen Che, Chun-li Wang, Song-ming Huang

    Diterbitkan 2024-05-01
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