Search

Jiewei Luo*

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
Mutational analysis of a familial adenomatous polyposis pedigree with bile duct polyp phenotype
Analysis of mutations in six Chinese families with autosomal dominant polycystic kidney disease