Kawai, C., Minatogawa, Y., Akiyoshi, H., Hirose, S., Suehiro, T., & Tone, S. (2012). A Novel Mutation of Human Liver Alanine: Glyoxylate Aminotransferase Causes Primary Hyperoxaluria Type 1: Immunohistochemical Quantification and Subcellular Distribution. Japan Society of Histochemistry and Cytochemistry.

Kawai, Chikage, Yohsuke Minatogawa, Hidetaka Akiyoshi, Shinichi Hirose, Tsunatoshi Suehiro, et Shigenobu Tone. A Novel Mutation of Human Liver Alanine: Glyoxylate Aminotransferase Causes Primary Hyperoxaluria Type 1: Immunohistochemical Quantification and Subcellular Distribution. Japan Society of Histochemistry and Cytochemistry, 2012.

Kawai, Chikage, et al. A Novel Mutation of Human Liver Alanine: Glyoxylate Aminotransferase Causes Primary Hyperoxaluria Type 1: Immunohistochemical Quantification and Subcellular Distribution. Japan Society of Histochemistry and Cytochemistry, 2012.