APA

Yorifuji T., Kawakita R., Nagai S., Sugimine A., Doi H., Nomura A., Masue M., Nishibori H., Yoshizawa A., Okamoto S., Doi R., Uemoto S. & Nagasaka H. (20110204). Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes. : The Journal of clinical endocrinology and metabolism.

Chicago

Yorifuji Tohru, Kawakita Rie, Nagai Shizuyo, Sugimine Akinori, Doi Hiraku, Nomura Anryu, Masue Michiya, Nishibori Hironori, Yoshizawa Akihiko, Okamoto Shinya, Doi Ryuichiro, Uemoto Shinji and Nagasaka Hironori. 20110204. Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes. : The Journal of clinical endocrinology and metabolism.

Harvard

Yorifuji T., Kawakita R., Nagai S., Sugimine A., Doi H., Nomura A., Masue M., Nishibori H., Yoshizawa A., Okamoto S., Doi R., Uemoto S. and Nagasaka H. (20110204). Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes. : The Journal of clinical endocrinology and metabolism.

MLA

Yorifuji Tohru, Kawakita Rie, Nagai Shizuyo, Sugimine Akinori, Doi Hiraku, Nomura Anryu, Masue Michiya, Nishibori Hironori, Yoshizawa Akihiko, Okamoto Shinya, Doi Ryuichiro, Uemoto Shinji and Nagasaka Hironori. Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes. : The Journal of clinical endocrinology and metabolism. 20110204.