APA

Higasa K., Manabe J. I., Yubisui T., Sumimoto H., Pung-Amritt P., Tanphaichitr V. S. & Fukumaki Y. (19990219). Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH-cytochrome b5 reductase gene. : British journal of haematology.

Chicago

Higasa K, Manabe J I, Yubisui T, Sumimoto H, Pung-Amritt P, Tanphaichitr V S and Fukumaki Y. 19990219. Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH-cytochrome b5 reductase gene. : British journal of haematology.

Harvard

Higasa K., Manabe J. I., Yubisui T., Sumimoto H., Pung-Amritt P., Tanphaichitr V. S. and Fukumaki Y. (19990219). Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH-cytochrome b5 reductase gene. : British journal of haematology.

MLA

Higasa K, Manabe J I, Yubisui T, Sumimoto H, Pung-Amritt P, Tanphaichitr V S and Fukumaki Y. Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH-cytochrome b5 reductase gene. : British journal of haematology. 19990219.