A unique 502C>T mutation in exon 7 of ABO gene associated with the Bel phenotype in Taiwan

Transfusion

Volumn 43, Issue 9, 2003, Pages 1254-1259

  Lin, P H ^b   Li, L ^b   Lin Tsai, S J ^b   Lin, K T ^b   Chen, J M ^b   Chu, Da Chang ^a  

^a CHANG GUNG UNIVERSITY   (Taiwan)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD GROUP A ANTIBODY; BLOOD GROUP B ANTIBODY;

ABO GENE; ARTICLE; BLOOD ANALYSIS; BLOOD DONOR; BLOOD GROUP ABO SYSTEM; DNA SEQUENCE; EXON; GENE; GENE AMPLIFICATION; GENE MUTATION; GENOTYPE; HUMAN; MOLECULAR DYNAMICS; PHENOTYPE; RESTRICTION SITE; SERODIAGNOSIS; TAIWAN;

ABO BLOOD-GROUP SYSTEM; ALLELES; BLOOD DONORS; DNA MUTATIONAL ANALYSIS; EXONS; GENOTYPE; HUMANS; PHENOTYPE; POINT MUTATION; TAIWAN;

EID: 0041833754     PISSN: 00411132     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1537-2995.2003.00494.x     Document Type: Article

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