APA

Shigemoto M., Yoshimasa Y., Yamamoto Y., Hayashi T., Suga J., Inoue G., Okamoto M., Jingami H., Tsuda K., Yamamoto T., Yagura T., Oishi M., Tsujii S., Kuzuya H. & Nakao K. (19980727). Clinical manifestations due to a point mutation of the mitochondrial tRNAleu(UUR) gene in five families with diabetes mellitus. : Internal medicine (Tokyo, Japan).

Chicago

Shigemoto M, Yoshimasa Y, Yamamoto Y, Hayashi T, Suga J, Inoue G, Okamoto M, Jingami H, Tsuda K, Yamamoto T, Yagura T, Oishi M, Tsujii S, Kuzuya H and Nakao K. 19980727. Clinical manifestations due to a point mutation of the mitochondrial tRNAleu(UUR) gene in five families with diabetes mellitus. : Internal medicine (Tokyo, Japan).

Harvard

Shigemoto M., Yoshimasa Y., Yamamoto Y., Hayashi T., Suga J., Inoue G., Okamoto M., Jingami H., Tsuda K., Yamamoto T., Yagura T., Oishi M., Tsujii S., Kuzuya H. and Nakao K. (19980727). Clinical manifestations due to a point mutation of the mitochondrial tRNAleu(UUR) gene in five families with diabetes mellitus. : Internal medicine (Tokyo, Japan).

MLA

Shigemoto M, Yoshimasa Y, Yamamoto Y, Hayashi T, Suga J, Inoue G, Okamoto M, Jingami H, Tsuda K, Yamamoto T, Yagura T, Oishi M, Tsujii S, Kuzuya H and Nakao K. Clinical manifestations due to a point mutation of the mitochondrial tRNAleu(UUR) gene in five families with diabetes mellitus. : Internal medicine (Tokyo, Japan). 19980727.