Cite
Common mutations F310L and T1559del in the tissue-nonspecific alkaline phosphatase gene are related to distinct phenotypes in Japanese patients with hypophosphatasia.
MLA
Michigami, Toshimi, et al. “Common Mutations F310L and T1559del in the Tissue-Nonspecific Alkaline Phosphatase Gene Are Related to Distinct Phenotypes in Japanese Patients with Hypophosphatasia.” European Journal of Pediatrics, vol. 164, no. 5, May 2005, pp. 277–82. EBSCOhost, https://doi.org/10.1007/s00431-004-1612-9.
APA
Michigami, T., Uchihashi, T., Suzuki, A., Tachikawa, K., Nakajima, S., & Ozono, K. (2005). Common mutations F310L and T1559del in the tissue-nonspecific alkaline phosphatase gene are related to distinct phenotypes in Japanese patients with hypophosphatasia. European Journal of Pediatrics, 164(5), 277–282. https://doi.org/10.1007/s00431-004-1612-9
Chicago
Michigami, Toshimi, Takayuki Uchihashi, Akira Suzuki, Kanako Tachikawa, Shigeo Nakajima, and Keiichi Ozono. 2005. “Common Mutations F310L and T1559del in the Tissue-Nonspecific Alkaline Phosphatase Gene Are Related to Distinct Phenotypes in Japanese Patients with Hypophosphatasia.” European Journal of Pediatrics 164 (5): 277–82. doi:10.1007/s00431-004-1612-9.