Recessive hereditary methemoglobinemia: Two novel mutations in the NADH-cytochrome b5 reductase gene-Reference-Cited by-同舟云学术

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Recessive hereditary methemoglobinemia: Two novel mutations in the NADH-cytochrome b5 reductase gene

Published:2008-07 Issue:1 Volume:41 Page:50-55
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Fermo Elisa,Bianchi Paola,Vercellati Cristina,Marcello Anna Paola,Garatti Massimo,Marangoni Ornella,Barcellini Wilma,Zanella Alberto

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference47 articles.

1. Soluble cytochrome b5 reductase from human erythrocytes;Passon;Biochim. Biophys. Acta,1972

2. Catalysis of methaemoglobin reduction by erythrocyte cytochrome b5 and cytochrome b5 reductase;Hultquist;Nature New Biol.,1971

3. Distribution of the integral membrane protein NADH-cytochrome b5 reductase in rat liver cells, studied with a quantitative radioblotting assay;Borgese;Biochem. J.,1986

4. A function of cytochrome b5 in fatty acid desaturation by rat liver microsomes;Oshino;J. Biochem.,1971

5. Biochemical properties of cytochrome b5-dependent microsomal fatty acid elongation and identification of products;Keyes;J. Biol. Chem.,1980

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