Alteration of NADH-diaphorase and cytochrome b5 reductase activities of erythrocytes, platelets, and leucocytes in hereditary methaemoglobinaemia with and without mental retardation.

Author:

Takeshita M,Matsuki T,Tanishima K,Yubisui T,Yoneyama Y,Kurata K,Hara N,Igarashi T

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. Purification of reduced pyridine nucleotide dehydrogenase from human erythrocytes and methemoglobin reduction by the enzyme;Sugita, Y.; Nomura, S.; Yoneyama, Y.;J Biol Chem; dependent on FAD has been reported.28 The physiological role of these diaphorases, apart from the DIA1 product, is not yet clear. The 'red cell' type diaphorase has been demonstrated in a variety of,1971

2. Catalysis of methemoglobin reduction by erythrocyte cytochrome br and cytochrome b5 reductase;Hultquist, D.E.; Passon, P.G.;Nature,1971

3. Hereditary methemoglobinemia with deficiency of NADH dehydrogenase;Schwarz, J.M.; Jaffe, E.R.,1978

4. Mental retardation in methemoglobinemia due to diaphorase deficiency;Fialkow, B.J.; Brower, J.A.; Sparkes, R.S.; Motuisky, A.G.;N Engl J Med,1965

5. Meth6moglobin6mie h6r6diteire avec arri6ration mentale;Heusden, A.; Willems, C.; Lambotte, C.; Hainaut, H.; Chapelle, P.; Malchair, R.;Arch Fr Pediatr,1971

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