论文信息 - Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH‐cytochrome b5 reductase gene - 字舞流文

Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH‐cytochrome b5 reductase gene

K. Higasa | Y. Fukumaki | H. Sumimoto | V. Tanphaichitr | P. Pung‐amritt | J. Manabe | Toshitsuga Yubisui | Varavarn S. Tanphaichitr