Biochemical and genetic basis of red cell enzyme deficiencies

Best Practice and Research: Clinical Haematology

Volumn 13, Issue 1, 2000, Pages 1-20

  Jacobasch, Gisela ^a  

^a GERMAN INSTITUTE OF HUMAN NUTRITION   (Germany)

Author keywords

Enzyme deficiencies; Erythrocyte; Haemolytic anaemia; Metabolic impairment; Mutations; Polymorphic sites; Secondary haemochromatosis

Indexed keywords

6 PHOSPHOFRUCTOKINASE; ADENOSINE DEAMINASE; ADENYLATE KINASE; BISPHOSPHOGLYCERATE MUTASE; CHELATING AGENT; ENOLASE; FREE RADICAL; FRUCTOSE BISPHOSPHATE ALDOLASE; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; GLUCOSE 6 PHOSPHATE ISOMERASE; GLUTATHIONE; GLUTATHIONE PEROXIDASE; GLUTATHIONE REDUCTASE; HEXOKINASE; IRON; LACTATE DEHYDROGENASE; PHOSPHOGLYCERATE KINASE; PYRIMIDINE 5' NUCLEOTIDE NUCLEOSIDASE; PYRUVATE KINASE; TRIOSEPHOSPHATE ISOMERASE;

BIOCHEMISTRY; CELL LEVEL; CELLULAR PARAMETERS; CHRONIC DISEASE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE SEVERITY; ENZYME DEFICIENCY; ERYTHROCYTE DISORDER; ERYTHROCYTE FUNCTION AND CHARACTERISTICS; EXERCISE; FAVISM; FEVER; GENE DELETION; GENE INSERTION; GENE SEQUENCE; GENETIC CODE; GENETICS; GEOGRAPHIC DISTRIBUTION; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; GLUTATHIONE METABOLISM; HEMOCHROMATOSIS; HEMOLYSIS; HEMOLYTIC ANEMIA; HUMAN; INFECTION; MISSENSE MUTATION; MORTALITY; PREVENTION; PRIORITY JOURNAL; PROMOTER REGION; REVIEW; STOP CODON;

EID: 0034429955     PISSN: 15216926     EISSN: None     Source Type: Journal    
DOI: 10.1053/beha.2000.0054     Document Type: Article

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