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Dive into the research topics of 'A novel mutation in CLDN16 results in rare familial hypomagnesaemia with hypercalciuria and nephrocalcinosis in a Chinese family'. Together they form a unique fingerprint.- Sort by
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Fang Lv, Xiao jie Xu, Jian yi Wang, Yi Liu, Yan Jiang, Ou Wang, Wei bo Xia, Xiao ping Xing, Mei Li*
Research output: Contribution to journal › Article › peer-review