Influence of BCL11A, HBS1L-MYB, HBBP1 single nucleotide polymorphisms and the HBG2 XmnI polymorphism on Hb F levels

Hemoglobin

Volumn 36, Issue 6, 2012, Pages 592-599

  Roy, Papai ^a   Bhattacharya, Gargi ^a   Mandal, Amrita ^a   Dasgupta, Uma B ^a   Banerjee, Debasis ^b   Chandra, Sarmila ^b   Das, Manikanchan ^b  

^a UNIVERSITY OF CALCUTTA   (India)

^b Park Clinic   (India)

Author keywords

Fetal hemoglobin (Hb F); HBBP1; India; Thalassemia; Trans polymorphisms

Indexed keywords

HEMOGLOBIN BETA CHAIN; HEMOGLOBIN F; MEMBRANE PROTEIN; PROTEIN BCL11A; PROTEIN HBBP1; PROTEIN HBG2; PROTEIN HBSL1L MYB; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; CHROMOSOME 11; CHROMOSOME 2; CHROMOSOME ANALYSIS; CONTROLLED STUDY; FEMALE; GENE DELETION; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC SCREENING; HEMOGLOBIN BLOOD LEVEL; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; PHENOTYPE; POINT MUTATION; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PROMOTER REGION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SCHOOL CHILD; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; THALASSEMIA;

ADOLESCENT; ADULT; ANEMIA, SICKLE CELL; BETA-GLOBINS; CARRIER PROTEINS; CHILD; CHILD, PRESCHOOL; DNA, INTERGENIC; FEMALE; FETAL HEMOGLOBIN; GAMMA-GLOBINS; GENES, MYB; HUMANS; INDIA; INFANT; MALE; MIDDLE AGED; MUTATION; NUCLEAR PROTEINS; PHENOTYPE; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; YOUNG ADULT;

EID: 84870276596     PISSN: 03630269     EISSN: 1532432X     Source Type: Journal    
DOI: 10.3109/03630269.2012.735626     Document Type: Article

References (12)

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