A microplate reader-based method to quantify NADH-cytochrome b5 reductase activity for diagnosis of recessive congenital methaemoglobinemia
Author:
Affiliation:
1. National Institute of Immunohematology (Indian Council of Medical Research), Mumbai, India
Funder
Indian Council of Medical Research
Publisher
Informa UK Limited
Subject
Hematology,Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/10245332.2016.1252873
Reference16 articles.
1. The enzymic defect of hereditary methemoglobinemia: diaphorase
2. NADH-ferricyanide reductase, a convenient approach to the evaluation of nadh-methaemoglobin reductase in human erythrocytes
3. Electrophoresis of red cell NADH- and NADPH-diaphorases in normal subjects and patients with congenital methemoglobinemia
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