APA

Nagasaki K., Usui T., Asami T., Ogawa Y., Kikuchi T. & Uchiyama M. (20130808). H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency. : Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Chicago

Nagasaki Keisuke, Usui Takeshi, Asami Tadashi, Ogawa Yohei, Kikuchi Toru and Uchiyama Makoto. 20130808. H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency. : Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Harvard

Nagasaki K., Usui T., Asami T., Ogawa Y., Kikuchi T. and Uchiyama M. (20130808). H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency. : Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

MLA

Nagasaki Keisuke, Usui Takeshi, Asami Tadashi, Ogawa Yohei, Kikuchi Toru and Uchiyama Makoto. H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency. : Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology. 20130808.