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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype
Chenchen Feng1, Hui Li2, Taixiang Liu1
1Transfusion Research Department, Jiangsu Province Blood Center, Nanjing, China.
Transfusion
|July 29, 2021
Abstract
No abstract available in PubMed .
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