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Article

A novel variant DO*A allele with a c.370delT mutation leading to a DO-null phenotype in a Syrian family.

Transfusion - 1 Feb 2021

Morin Pierre-Aurèle, Ethier Carole, Lavoie Josée, Robitaille Nancy, Baillargeon Nadia

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PMID: 33206405
DOI: 10.1111/trf.16193

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