Hb Paksé [(α2) codon 142 (TAA→TAT or Term→Tyr)] in Thai patients with EABart's disease and Hb H disease

Hemoglobin

Volumn 26, Issue 3, 2002, Pages 227-235

  Sanchaisuriya, Kanokwan ^a   Fucharoen, Goonnapa ^a   Fucharoen, Supan ^a  

^a KHON KAEN UNIVERSITY   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLOBIN; GLYCINE; HEMOGLOBIN H; HEMOGLOBIN PAKSE; HEMOGLOBIN VARIANT; TYROSINE; UNCLASSIFIED DRUG; HEMOGLOBIN BART'S;

ADOLESCENT; ADULT; ALLELE; ALPHA THALASSEMIA; ARTICLE; ASSAY; CHILD; CLINICAL ARTICLE; EABART SYNDROME; GENE MUTATION; HEMOGLOBIN CONSTANT SPRING; HEMOGLOBINOPATHY; HUMAN; HUMAN TISSUE; INHERITANCE; POLYMERASE CHAIN REACTION; SCREENING; SCREENING TEST; STOP CODON; SYNDROME; THAILAND; VALIDATION PROCESS; GENETICS; INFANT; MASS SCREENING; METHODOLOGY; PRESCHOOL CHILD; VALIDATION STUDY;

LAOTIA;

ADOLESCENT; ADULT; ALLELES; ALPHA-THALASSEMIA; CHILD; CHILD, PRESCHOOL; HEMOGLOBINOPATHIES; HEMOGLOBINS, ABNORMAL; HUMANS; INFANT; MASS SCREENING; POLYMERASE CHAIN REACTION; THAILAND;

EID: 0036402894     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.1081/HEM-120015026     Document Type: Article

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