Literature DB >> 4144157

Hereditary methemoglobinemia associated with NADH diaphorase deficiency.

H Ritter, K Schmidt, J Schmitt.   

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Year:  1973        PMID： 4144157     DOI： 10.1007/bf00277915

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  5 in total

1.  Electrophoresis of red cell NADH- and NADPH-diaphorases in normal subjects and patients with congenital methemoglobinemia.

Authors:  J C Kaplan; E Beutler
Journal:  Biochem Biophys Res Commun       Date:  1967-11-30       Impact factor: 3.575

2.  [Genetically determined variants of NADH-diaphorase].

Authors:  G Tariverdian; H Ritter; G G Wendt
Journal:  Humangenetik       Date:  1970

3.  NADH diaphorase: an inherited variant associated with normal methemoglobin reduction.

Authors:  J C Detter; J E Anderson; E R Giblett
Journal:  Am J Hum Genet       Date:  1970-01       Impact factor: 11.025

4.  Demonstration of an enzyme variant in a case of congenital methaemoglobinaemia.

Authors:  C A West; B D Gomperts; E R Huehns; I Kessel; J R Ashby
Journal:  Br Med J       Date:  1967-10-28

5.  A starch-gel electrophoretic method for the study of diaphorase isozymes and preliminary results with sheep and human erythrocytes.

Authors:  G J Brewer; J W Eaton; C S Knutsen; C C Beck
Journal:  Biochem Biophys Res Commun       Date:  1967-10-26       Impact factor: 3.575
  5 in total

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