Decrease of palmitoyl-CoA elongation in platelets and leukocytes in the patient of hereditary methemoglobinemia associated with mental retardation
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference20 articles.
1. The Metabolic Basis of Inherited Disease;Schwartz,1983
2. Alteration of NADH-diaphorase and cytochrome b5 reductase activities of erythrocytes, platelets, and leucocytes in hereditary methaemoglobinaemia with and without mental retardation.
3. Generalised deficiency of cytochrome b5 reductase in congenital methaemoglobinaemia with mental retardation
4. Hereditary methemoglobinemia due to cytochrome b5 reductase deficiency in blood cells without associated neurologic and mental disorders
5. Complete Amino Acid Sequence of NADH-Cytochrome b5 Reductase Purified from Human Erythrocytes1
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia;Human Mutation;2020-01-30
2. Methemoglobinemia;American Journal of Hematology;1993-01
3. Evidence against cytochrome b5 involvement in liver microsomal fatty acid elongation;Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism;1991-02
4. Effect of divalent cations on NADH-dependent and NADPH-dependent cytochrome b5 reduction by hepatic microsomes;Archives of Biochemistry and Biophysics;1990-08
5. Characterization of fatty acid elongation system in porcine neutrophil microsomes;Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism;1990-03
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