Literature DB >> 29468689

A novel variant B allele at the ABO gene locus characterized by a duplication-based insertion of 27 nucleotides identified in an Iraqi male with a weak B subgroup phenotype.

Eva Maria Matzhold1, Camilla Drexler1, Erika Staudacher2, Barbara Glock3, Thomas Wagner1.   

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Year:  2018        PMID： 29468689     DOI： 10.1111/trf.14539

Source DB:  PubMed          Journal:  Transfusion        ISSN： 0041-1132            Impact factor:   3.157


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  2 in total

1.  A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O.

Authors:  Eva Maria Matzhold; Camilla Drexler; Andrea Wagner; Claudia Bernecker; Ariane Pessentheiner; Juliane Gertrude Bogner-Strauß; Wolfgang Helmberg; Thomas Wagner
Journal:  Transfusion       Date:  2020-06-04       Impact factor: 3.157

2.  Aberrant ABO B Phenotype with Irregular Anti-B Caused by a Para-Bombay FUT1 Mutation.

Authors:  Eva Maria Matzhold; Thomas Wagner; Camilla Drexler; Marlies Schönbacher; Günther F Körmöczi
Journal:  Transfus Med Hemother       Date:  2019-04-29       Impact factor: 3.747
  2 in total

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