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.
Takanori Katsube(National Institutes for Quantum Science and Technology), M Takeshita(University of Miyazaki), Akio Tomoda(Tokyo Medical University), Ryohei Seki, N Sakamoto, T Yubisui, Kiyoh Tanishima, Eisuke Takazakura, M Hirano, Yasushi Kobayashi(National Defense Medical College)
PubMed
April 1, 1991
Cited by 40
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