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Bungard D, Fuerth BJ, Zeng PY, et al
These findings highlight the importance of considering donor enzymatic status in transfusion practice and underscore the need for further research into screening strategies and storage optimization for G6PD-deficient units
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Viral growth, titration, purification, and inactivation Once viruses were recovered, they were grown on Vero CCL81 cells in viral production serum-free medium (VP-SFM) (Thermo Fisher) supplemented with 5% Glutamax, 1% penicillin-streptomycin, and 1% HEPES buffers
