Detection of Hpdel among Thais, a deleted allele of the haptoglobin gene that causes congenital haptoglobin deficiency

Transfusion

Volumn 47, Issue 12, 2007, Pages 2315-2321

  Shimada, Eiko ^a   Odagiri, Miki ^b   Chaiwong, Kriangsak ^b   Watanabe, Yoshihisa ^b   Anazawa, Masako ^b   Mazda, Toshio ^b   Okazaki, Hitoshi ^b   Juji, Takeo ^b   O'Charoen, Rachanee ^b   Tadokoro, Kenji ^b  

^a SUWA RED CROSS HOSPITAL   (Japan)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; HAPTOGLOBIN; HP PROTEIN, HUMAN; UNCLASSIFIED DRUG;

ALLELE; ANAPHYLAXIS; ARTICLE; BLOOD SAMPLING; CONTROLLED STUDY; GENE FREQUENCY; HAPTOGLOBIN DEFICIENCY; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN EXPERIMENT; HUMAN TISSUE; NORMAL HUMAN; PHENOTYPE; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERASE CHAIN REACTION; PREVALENCE; PROTEIN BLOOD LEVEL; PROTEIN DEFICIENCY; RISK FACTOR; SOUTHEAST ASIA; THAILAND; WESTERN BLOTTING; ASIAN; ENZYME LINKED IMMUNOSORBENT ASSAY; ETHNOLOGY; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETICS; HOMOZYGOTE; JAPAN;

ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; ENZYME-LINKED IMMUNOSORBENT ASSAY; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HAPTOGLOBINS; HOMOZYGOTE; HUMANS; JAPAN; PHENOTYPE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; THAILAND;

EID: 36348950193     PISSN: 00411132     EISSN: 15372995     Source Type: Journal    
DOI: 10.1111/j.1537-2995.2007.01473.x     Document Type: Article

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