ABO exon and intron analysis in individuals with the A(weak)B phenotype reveals a novel O(1v)-A(2 )hybrid allele that causes four missense mutations in the A transferase

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 t...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Hosseini-Maaf, Bahram, Hellberg, Åsa, Rodrigues, Maria J, Chester, M Alan, Olsson, Martin L
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2003
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC305365/
https://ncbi.nlm.nih.gov/pubmed/14617382
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-4-17
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