Clinical and hematologic features of β0-thalassemia (frameshift 41/42 mutation) in Thai patients

Haematologica

Volumn 86, Issue 2, 2001, Pages 138-141

  Laosombat, V ^a   Wongchanchailert, M ^a   Sattayasevana, B ^a   Wiriyasateinkul, A ^a   Fucharoen, S ^a  

^a THAMMASAT UNIVERSITY   (Thailand)

Author keywords

0 thalassemia; Frameshift 41 42 mutation; Genotype; Phenotype

Indexed keywords

ARTICLE; BETA THALASSEMIA; CLINICAL FEATURE; DISEASE SEVERITY; DNA POLYMORPHISM; FRAMESHIFT MUTATION; GENETIC ANALYSIS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INFANT; MAJOR CLINICAL STUDY; PHENOTYPE; PRESCHOOL CHILD; SCHOOL CHILD;

ALLELES; BETA-THALASSEMIA; CHILD; CHILD, PRESCHOOL; FRAMESHIFT MUTATION; HEMOGLOBIN E; HUMANS; PHENOTYPE; SEVERITY OF ILLNESS INDEX; THAILAND;

EID: 0035100012     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (16)

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8. Molecular basis of Hb E-β-thalassemia and the origin of Hb E in northeast Thailand: Identification of one novel mutation using amplified DNA from buffy coat specimens
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16. Severity differences in β-thalassemia haemoglobin E syndromes: Implication of genetic factors