Nagasaki, K., Usui, T., Asami, T., Ogawa, Y., Kikuchi, T., & Uchiyama, M. (2009). H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency. The Japanese Society for Pediatric Endocrinology.

Nagasaki, Keisuke, Takeshi Usui, Tadashi Asami, Yohei Ogawa, Toru Kikuchi, i Makoto Uchiyama. H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency. The Japanese Society for Pediatric Endocrinology, 2009.

Nagasaki, Keisuke, et al. H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency. The Japanese Society for Pediatric Endocrinology, 2009.