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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1992 | 1 |
2004 | 1 |
2005 | 1 |
2024 | 0 |
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Enzymatic instability of NADH-cytochrome b5 reductase as a cause of hereditary methemoglobinemia type I (red cell type).
J Biol Chem. 1992 Oct 5;267(28):20416-21.
J Biol Chem. 1992.
PMID: 1400360
Free article.
Structure of human erythrocyte NADH-cytochrome b5 reductase.
Bando S, Takano T, Yubisui T, Shirabe K, Takeshita M, Nakagawa A.
Bando S, et al.
Acta Crystallogr D Biol Crystallogr. 2004 Nov;60(Pt 11):1929-34. doi: 10.1107/S0907444904020645. Epub 2004 Oct 20.
Acta Crystallogr D Biol Crystallogr. 2004.
PMID: 15502298
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Recessive congenital methaemoglobinaemia: functional characterization of the novel D239G mutation in the NADH-binding lobe of cytochrome b5 reductase.
Percy MJ, Crowley LJ, Davis CA, McMullin MF, Savage G, Hughes J, McMahon C, Quinn RJ, Smith O, Barber MJ, Lappin TR.
Percy MJ, et al.
Br J Haematol. 2005 Jun;129(6):847-53. doi: 10.1111/j.1365-2141.2005.05526.x.
Br J Haematol. 2005.
PMID: 15953014
Free article.
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