A novel Aγδβ0-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization

Clinical Biochemistry

Volumn 48, Issue 10-11, 2015, Pages 703-708

  Singha, Kritsada ^a   Fucharoen, Goonnapa ^a   Hama, Abdulloh ^b   Fucharoen, Supan ^a  

^a KHON KAEN UNIVERSITY   (Thailand)

^b Narathiwasrajanagarindra Hospital   (Thailand)

Author keywords

A 0 Thalassemia; Hereditary persistence of fetal hemoglobin (HPFH); High hemoglobin F determinant; Olfactory receptor gene deletion

Indexed keywords

HEMOGLOBIN BETA CHAIN; HEMOGLOBIN E; HEMOGLOBIN F; OR51A1P PROTEIN; OR51V1 PROTEIN; OR52A1 PROTEIN; OR52A5 PROTEIN; OR52Z1 PROTEIN; PROTEIN; UNCLASSIFIED DRUG;

ADULT; ARTICLE; BETA THALASSEMIA; CAPILLARY ELECTROPHORESIS; CLINICAL ARTICLE; CONTROLLED STUDY; DELTA THALASSEMIA; DNA DETERMINATION; DNA SEQUENCE; FEMALE; GAMMA DELTA BETA THALASSEMIA; GENE CLUSTER; GENE INSERTION SEQUENCE; GENE INTERACTION; GENOTYPE; HAPLOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; INVERSION INSERTION SEQUENCE; MALE; MEAN CORPUSCULAR VOLUME; MULTIPLEX POLYMERASE CHAIN REACTION; OLFACTORY RECEPTOR; PHENOTYPE; PRIORITY JOURNAL; THAILAND; ALPHA-THALASSEMIA; BETA-THALASSEMIA; CASE REPORT; CHROMOSOME INVERSION; DELTA-THALASSEMIA; EPISTASIS; GENE DELETION; GENE EXPRESSION REGULATION; GENETICS; MIDDLE AGED; MOLECULAR GENETICS; MULTIGENE FAMILY; NUCLEOTIDE SEQUENCE; OLFACTORY RECEPTOR NEURON; PEDIGREE; PHYSIOLOGY; YOUNG ADULT;

ADULT; ALPHA-THALASSEMIA; BASE SEQUENCE; BETA-GLOBINS; BETA-THALASSEMIA; CHROMOSOME INVERSION; DELTA-THALASSEMIA; EPISTASIS, GENETIC; FEMALE; GENE DELETION; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MULTIGENE FAMILY; MUTAGENESIS, INSERTIONAL; OLFACTORY RECEPTOR NEURONS; PEDIGREE; PHENOTYPE; YOUNG ADULT;

EID: 84939417567     PISSN: 00099120     EISSN: 18732933     Source Type: Journal    
DOI: 10.1016/j.clinbiochem.2015.03.023     Document Type: Article

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