Chronic haemolytic anaemia and glucose-6-phosphate dehydrogenase deficiency: Case report and review of the literature

Acta Haematologica

Volumn 108, Issue 2, 2002, Pages 102-105

  Hundsdoerfer, Patrick ^a   Vetter, B ^a   Kulozik, A E ^b  

^a HUMBOLDT UNIVERSITY   (Germany)

^b UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

Chronic haemolytic anaemia; Glucose 6 phosphate dehydrogenase deficiency

Indexed keywords

ANTIBIOTIC AGENT; NUCLEOTIDE;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANTIBIOTIC THERAPY; ARTICLE; CASE REPORT; CHROMOSOME XQ; DIMERIZATION; DISEASE ASSOCIATION; DNA DETERMINATION; ENZYME ACTIVITY; ENZYME STABILITY; ERYTHROCYTE TRANSFUSION; EXON; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEMOLYTIC ANEMIA; HUMAN; MALE; NEWBORN JAUNDICE; PRIORITY JOURNAL; RETICULOCYTOSIS; SEPTICEMIA; SPLENOMEGALY;

ADOLESCENT; AMINO ACID SUBSTITUTION; ANEMIA, HEMOLYTIC, CONGENITAL; CHRONIC DISEASE; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; HUMANS; MALE; POINT MUTATION;

EID: 0036373677     PISSN: 00015792     EISSN: None     Source Type: Journal    
DOI: 10.1159/000064749     Document Type: Article

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15. Four new electrophoretically slow-moving glucose 6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: Gd(-) Kurume, Gd(-) Fukushima, Gd(-) Yamaguchi and Gd(-) Wakayama
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