Gγ-37 (A→T): A new nondeletional hereditary persistence of fetal hemoglobin determinant associated with the rare codon 91 (+T) δ0 -thalassemia

Hemoglobin

Volumn 30, Issue 3, 2006, Pages 371-377

  Bouva, Marelle J ^a   Harteveld, Cornelis L ^a   Bakker Verweij, Greet ^a   Van Delft, Peter ^a   Giordano, Piero C ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Thalassemia (thal); Hb A2; Hb F; Hemoglobin (Hb); Nondeletional hereditary persistence of fetal hemoglobin (HPFH)

Indexed keywords

DELTA GLOBIN; GAMMA GLOBIN; HEMOGLOBIN F; IMMUNOGLOBULIN; THALASSEMIA GAMMA; UNCLASSIFIED DRUG; GLOBIN;

ADULT; ARTICLE; BELGIUM; CODON; CONTROLLED STUDY; DELTA THALASSEMIA; FEMALE; FRAMESHIFT MUTATION; GENE; GENE DELETION; GENE MUTATION; GENETIC LINKAGE; HAPLOTYPE; HEMOGLOBIN DETERMINATION; HUMAN; HUMAN TISSUE; INFANT; MALE; PRESCHOOL CHILD; PROMOTER REGION; PROTEIN ANALYSIS; PROTEIN EXPRESSION; THALASSEMIA; CASE REPORT; DNA SEQUENCE; GENETIC POLYMORPHISM; GENETICS; HEREDITARY SPHEROCYTOSIS; MIDDLE AGED; NUCLEOTIDE SEQUENCE; PEDIGREE;

ADULT; CHILD, PRESCHOOL; CODON; FEMALE; FETAL HEMOGLOBIN; FRAMESHIFT MUTATION; GLOBINS; HUMANS; INFANT; MALE; MIDDLE AGED; PEDIGREE; POLYMORPHISM, GENETIC; READING FRAMES; SEQUENCE ANALYSIS, DNA; SPHEROCYTOSIS, HEREDITARY; THALASSEMIA;

EID: 33746267903     PISSN: 03630269     EISSN: 1532432X     Source Type: Journal    
DOI: 10.1080/03630260600755641     Document Type: Article

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