Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH-cytochrome b5reductase gene
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1998.01123.x/fullpdf
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2. Role of Lys-110 of human NADH-cytochrome b5 reductase in NADH binding as probed by site-directed mutagenesis;Fujimoto;FEBS Letters,1993
3. The reduction of methemoglobin in red blood cells and studies on the cause of idiopathic methemoglobinemia;Gibson;Biochemical Journal,1948
4. Evidence for the participation of cytochrome b5 in hepatic microsomal mixed-function oxidation reactions;Hildebrandt;Archives of Biochemistry and Biophysics,1971
5. Site-directed mutagenesis by overlap extension using the PCR;Ho;Gene,1989
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