Relationship between molecular variants and clinical manifestions in twelve glucose-6-phosphate dehydrogenase-deficient patients in Jordan

Acta Haematologica

Volumn 114, Issue 2, 2005, Pages 125-126

  Karadsheh, Naif S ^a,e   Gelbart, Terri ^b   Schulten, Hans Jurgen ^c   Efferth, Thomas ^d   Awidi, Abdalla ^a  

^a THE UNIVERSITY OF JORDAN   (Jordan)

^b SCRIPPS RESEARCH INSTITUTE   (United States)

^c UNIVERSITY OF GÖTTINGEN   (Germany)

^d UNIVERSITY OF HEIDELBERG   (Germany)

^e UNIVERSITY OF JORDAN   (Jordan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; GLUCOSE 6 PHOSPHATE DEHYDROGENASE;

ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DNA POLYMORPHISM; ENZYME ACTIVITY; ENZYME ANALYSIS; GENE MUTATION; GENETIC ANALYSIS; GENETIC VARIABILITY; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEMOLYTIC ANEMIA; HUMAN; JORDAN; LABORATORY TEST; MOLECULAR GENETICS; MORBIDITY; MUTATIONAL ANALYSIS; PATIENT; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; VICIA FABA;

ANEMIA; FAVISM; FEMALE; GLUCOSEPHOSPHATE DEHYDROGENASE; HUMANS; INFANT, NEWBORN; JAUNDICE, NEONATAL; JORDAN; MALE; POINT MUTATION;

EID: 23844468458     PISSN: 00015792     EISSN: None     Source Type: Journal    
DOI: 10.1159/000086589     Document Type: Article

References (6)

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