APA Alıntı

Kawahara, T., Watanabe, H., Omae, R., Yamamoto, T., & Inazu, T. (2015). A Novel PHEX Mutation in Japanese Patients with X-Linked Hypophosphatemic Rickets. Case Rep Genet.

Chicago Stili Alıntı

Kawahara, Tetsuya, Hiromi Watanabe, Risa Omae, Toshiyuki Yamamoto, ve Tetsuya Inazu. "A Novel PHEX Mutation in Japanese Patients With X-Linked Hypophosphatemic Rickets." Case Rep Genet 2015.

MLA Alıntı

Kawahara, Tetsuya, et al. "A Novel PHEX Mutation in Japanese Patients With X-Linked Hypophosphatemic Rickets." Case Rep Genet 2015.