Literature DB >> 14075877

A DUAL HEREDITARY RED BLOOD CELL DEFECT IN ONE FAMILY: HYPOCATALASEMIA AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.

A SZEINBERG, A DE VRIES, J PINKHAS, M DJALDETTI, R EZRA.   

Abstract

Entities:  

Keywords:  ANEMIA, HEMOLYTIC; CATALASE; GENETICS, HUMAN; GLUCOSEPHOSPHATE DEHY- DROGENASE DEFICIENCY; IRAN; JEWS

Mesh：

Substances：

Year:  1963        PMID： 14075877     DOI： 10.1017/s1120962300016231

Source DB:  PubMed          Journal:  Acta Genet Med Gemellol (Roma)        ISSN： 0001-5660


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  5 in total

1.  Frequency of hypocatalasemia in a sample of Spanish population.

Authors:  A Pellicer; L Vicente; E Lopez; M De las Heras; A Casado
Journal:  Experientia       Date:  1975-01-15

Review 2.  Catalase enzyme mutations and their association with diseases.

Authors:  László Góth; Péter Rass; Anikó Páy
Journal:  Mol Diagn       Date:  2004

3.  Acatalasemia in the mouse and other species.

Authors:  R N Feinstein
Journal:  Biochem Genet       Date:  1970-02       Impact factor: 1.890

4.  Acatalasia discovered by accident during a disk operation.

Authors:  G Pflüger; E Kaiser
Journal:  Arch Orthop Trauma Surg       Date:  1988

Review 5.  Acatalasemia.

Authors:  M Ogata
Journal:  Hum Genet       Date:  1991-02       Impact factor: 4.132
  5 in total

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