<it>ABO </it>exon and intron analysis in individuals with the A<sub>weak</sub>B phenotype reveals a novel <it>O</it><sup>1<it>v</it></sup>-<it>A</it><sup>2 </sup>hybrid allele that causes four missense mutations in the A transferase
<p>Abstract</p> <p>Background</p> <p>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,...
Main Authors: | Chester M Alan, Rodrigues Maria J, Hellberg Åsa, Hosseini-Maaf Bahram, Olsson Martin L |
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Format: | Article |
Language: | English |
Published: |
BMC
2003-11-01
|
Series: | BMC Genetics |
Online Access: | http://www.biomedcentral.com/1471-2156/4/17 |
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