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Identification of a novel frameshift mutation in the SCNN1B causing Liddle syndrome.
Qu Y, Lu Y, Zhang D, Liu X, Fan P, Chen J, Zhang H, Yang K, Tian T, Zhou Y, Zhang Q, Zhang Y, Wang L, Huang Z, Liu Y, Hu A, Zhou X. Qu Y, et al. Among authors: zhang q, zhang d, zhang h, zhang y. Sci Bull (Beijing). 2023 Feb 26;68(4):383-387. doi: 10.1016/j.scib.2023.02.006. Epub 2023 Feb 7. Sci Bull (Beijing). 2023. PMID: 36774301 No abstract available.
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