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ABO exon and intron analysis in individuals with the AweakB phenotype reveals a novel O1v-A2 hybrid allele that causes four missense mutations in the A transferase
Authors:Bahram Hosseini-Maaf   ?sa Hellberg   Maria J Rodrigues   M Alan Chester  Martin L Olsson
Affiliation:(1) Dept. of Transfusion Medicine, Institute of Laboratory Medicine, Lund University & Blood Centre, University Hospital, SE-221 85 Lund, Sweden;(2) Centro Regional de Sangue de Lisboa/IPS, Lisboa, Portugal
Abstract:

Background  

Since the cloning in 1990 of cDNA corresponding to mRNA transcribed at the blood-group ABO locus, polymorphisms due to ethnic and/or phenotypic variations have been reported. Some subgroups have been explained at the molecular level, but unresolved samples are frequently encountered in the reference laboratory.
Keywords:
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