Literature DB >> 5170469

Studies on erythrocyte metabolism in a case with hereditary deficiency of H-subunit of lactate dehydrogenase.

S Miwa, T Nishina, Y Kakehashi, M Kitamura, A Hiratsuka.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1971        PMID： 5170469

Source DB:  PubMed          Journal:  Nihon Ketsueki Gakkai Zasshi        ISSN： 0001-5806


× No keyword cloud information.
  3 in total

1.  A mutation affecting the lactate dehydrogenase locus Ldh-1 in the mouse. II. Mechanism of the LDH-A deficiency associated with hemolytic anemia.

Authors:  W Pretsch; S Merkle; J Favor; T Werner
Journal:  Genetics       Date:  1993-09       Impact factor: 4.562

Review 2.  Diagnosis of red blood cell enzymopathies in infants, children and adolescents.

Authors:  S P Samuel; T D Miale
Journal:  Indian J Pediatr       Date:  1987 May-Jun       Impact factor: 1.967

Review 3.  [Enzyme deficiencies in glycolysis and nucleotide metabolism of red blood cells in nonspherocytic hemolytic anemia (author's transl)].

Authors:  H D Waller; H C Benöhr
Journal:  Klin Wochenschr       Date:  1976-09-01
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.