A novel G6PD mutation leading to chronic hemolytic anemia

Pediatric Blood and Cancer

Volumn 51, Issue 6, 2008, Pages 816-819

  McDade, Jenny ^a   Abramova, Tatiana ^a   Mortier, Nicole ^a   Howard, Thad ^a   Ware, Russell E ^a  

^a ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

Author keywords

G6PD deficiency; Hemolytic anemia

Indexed keywords

DNA; GLUCOSE 6 PHOSPHATE DEHYDROGENASE;

AFRICAN AMERICAN; ARTICLE; BLOOD ANALYSIS; CASE REPORT; CHRONIC DISEASE; CLINICAL FEATURE; CONTROLLED STUDY; DIMERIZATION; DISEASE ASSOCIATION; DISEASE COURSE; DNA SEQUENCE; ENZYME ACTIVITY; EXON; GENE MUTATION; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HAPLOTYPE; HEMOLYTIC ANEMIA; HUMAN; HUMAN CELL; JAUNDICE; MALE; OXIDATIVE STRESS; PALLOR; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; RESPIRATORY TRACT DISEASE;

ANEMIA, HEMOLYTIC; CHRONIC DISEASE; DNA; EXONS; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; HUMANS; INFANT, NEWBORN; MALE; MUTATION; POLYMERASE CHAIN REACTION;

EID: 56749182388     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.21715     Document Type: Article

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