Katsube, T., Sakamoto, N., Kobayashi, Y., Seki, R., Hirano, M., Tanishima, K., . . . Fukumaki, Y. (1991). Exonic point mutations in NADH-cytochrome B5 reductase genes of homozygotes for hereditary methemoglobinemia, types I and III: Putative mechanisms of tissue-dependent enzyme deficiency.
Citación estilo ChicagoKatsube, Takanori, et al. Exonic Point Mutations in NADH-cytochrome B5 Reductase Genes of Homozygotes for Hereditary Methemoglobinemia, Types I and III: Putative Mechanisms of Tissue-dependent Enzyme Deficiency. 1991.
Cita MLAKatsube, Takanori, et al. Exonic Point Mutations in NADH-cytochrome B5 Reductase Genes of Homozygotes for Hereditary Methemoglobinemia, Types I and III: Putative Mechanisms of Tissue-dependent Enzyme Deficiency. 1991.