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

A novel variant DO*A allele with a c.370delT mutation leading to a DO-null phenotype in a Syrian family. Transfusion. 2020 Nov 18;: Authors: Morin PA, Ethier C, Lavoie J, Robitaille N, Baillargeon N PMID: 33206405 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/33206405?dopt=Abstract

Source: Transfusion - November 18, 2020 Category: Hematology Authors: Morin PA, Ethier C, Lavoie J, Robitaille N, Baillargeon N Tags: Transfusion Source Type: research

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