APA (7th ed.) Citation

Sun, Y., Liu, Y., Zhang, X., & Jiang, L. Newly identified intronic and known pathogenic point mutations in SLC34A3/NPT2c cause hereditary hypophosphatemic rickets with hypercalciuria. KeAi Communications Co., Ltd.

Chicago Style (17th ed.) Citation

Sun, Yujing, Yuan Liu, Xiaoli Zhang, and Ling Jiang. Newly Identified Intronic and Known Pathogenic Point Mutations in SLC34A3/NPT2c Cause Hereditary Hypophosphatemic Rickets with Hypercalciuria. KeAi Communications Co., Ltd.

MLA (9th ed.) Citation

Sun, Yujing, et al. Newly Identified Intronic and Known Pathogenic Point Mutations in SLC34A3/NPT2c Cause Hereditary Hypophosphatemic Rickets with Hypercalciuria. KeAi Communications Co., Ltd.