Compound heterozygosity for α0-thalassemia (--THAI) and Hb constant spring causes severe Hb H disease

Hemoglobin

Volumn 26, Issue 2, 2002, Pages 155-162

  Viprakasit, Vip ^a,b   Tanphaichitr, Voravarn S ^b  

^a JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^b MAHIDOL UNIVERSITY   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLOBIN; HEMOGLOBIN H; HEMOGLOBIN CONSTANT SPRING; HEMOGLOBIN VARIANT;

ALPHA THALASSEMIA; ANEMIA; ARTICLE; CASE REPORT; DISEASE COURSE; DISEASE SEVERITY; FEMALE; GENE MUTATION; HEMOLYSIS; HETEROZYGOSITY; HUMAN; MALE; PHENOTYPE; PREVALENCE; RECURRENT DISEASE; SCHOOL CHILD; SCREENING; SPLENECTOMY; THAILAND; CHILD; GENE DELETION; GENETIC SCREENING; GENETICS; HETEROZYGOTE; INFANT; STOP CODON;

ALPHA-THALASSEMIA; CHILD; CODON, TERMINATOR; FEMALE; GENETIC SCREENING; HEMOGLOBINS, ABNORMAL; HETEROZYGOTE; HUMANS; INFANT; MALE; PHENOTYPE; SEQUENCE DELETION; THAILAND;

EID: 0036062574     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.1081/HEM-120005453     Document Type: Article

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