New variant of cytochrome b5 reductase deficiency (b5RKurashiki) in red cells, platelets, lymphocytes, and cultured fibroblasts with congenital methemoglobinemia, mental and neurological retardation, and skeletal anomalies
Author:
Publisher
Wiley
Subject
Hematology
Reference26 articles.
1. : Cytochrome b5 reductase deficiency and enzymopenic hereditary methemoglobinemia. In , , (eds): “The Metabolic Basis of Inherited Disease,” 6th ed. New York: McGraw-Hill, 1989, pp 2267–2280.
2. Characterization of the purified NADH-cytochrome b5 reductase of human erythrocytes as a FAD-containing enzyme.
3. Complete Amino Acid Sequence of NADH-Cytochrome b5 Reductase Purified from Human Erythrocytes1
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