Literature DB >> 5839175

Hereditary partial deficiency of human-erythrocyte phosphogluconate dehydrogenase.

C W Parr, L I Fitch.   

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Year:  1964        PMID： 5839175

Source DB:  PubMed          Journal:  Biochem J        ISSN： 0264-6021            Impact factor:   3.857


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  6 in total

1.  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

2.  [Phosphogluconate-dehydrogenase (PGD). Random sample of the Berlin population].

Authors:  M Smerling
Journal:  Z Rechtsmed       Date:  1971

3.  [Remarks on the stability of a variant at the 6-PGD locus (author's transl)].

Authors:  J Henke
Journal:  Z Rechtsmed       Date:  1979-08

Review 4.  [Red cell enzyme polymorphisms in forensic serology].

Authors:  B Brinkmann
Journal:  Z Rechtsmed       Date:  1971

5.  Biochemical and genetic characterization of the Lowell variant. A new phenotype of 6-phosphogluconate dehydrogenase.

Authors:  M S Nelson
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

6.  On the normal activites of glucose-6-phosphate dehydrogenase and 6-phospho-gluconate dehydrogenase in bovine erythrocytes.

Authors:  J Steensgaard
Journal:  Acta Vet Scand       Date:  1968       Impact factor: 1.695
  6 in total

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