Sheng Jiang

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1CO-AUTHORS
Cancer genetics
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Publications (1)

|Aug 19, 2025
Whole exome sequencing reveals a pathogenic homozygous CLDN16 mutation in a 17-year-old patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis: A case report.

Fei Wang, Yilinuer Adeerjiang, Hai-Qing Xing

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Yilinuer Adeerjiang