Related Experiment Video
Updated: Aug 15, 2025

06:41
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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c.5del mutation on the ABO*B.01 allele responsible for Bx phenotype
1Department of Transfusion, Shengjing Hospital of China Medical University, Shenyang, China.
Transfusion
|December 31, 2022
Abstract
No abstract available in PubMed .
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