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Jiabin Wu
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A study on the function of PH EX mutations p.Glul45* and p.Trp749Arg in families with X-linked hyphosphatemic rickets
Analysis of two pedigrees of Gitelman syndrome complicated with proteinuria or Hashimoto's thyroiditis caused by SLC12A3 compound heterozygous mutation and literature review
Analysis of mutations in six Chinese families with autosomal dominant polycystic kidney disease
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