A 3·0‐kb deletion including an erythroid cell‐specific regulatory element in intron 1 of the ABO blood group gene in an individual with the Bm phenotype

Publisher： John Wiley & Sons Inc

E-ISSN： 1423-0410|108|3|310-313

ISSN： 0042-9007

Source： VOX SANGUINIS, Vol.108, Iss.3, 2015-04, pp. : 310-313

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