Newly identified intronic and known pathogenic point mutations in SLC34A3/NPT2c cause hereditary hypophosphatemic rickets with hypercalciuria
Article in Genes & Diseases (May 2024)
The most recent citing publications are shown below. View all 18 publications that cite this research output on Dimensions.
Article in Genes & Diseases (May 2024)
Article in Kidney International (February 2024)
Article in Calcified Tissue International (November 2023)