Cite
HARVARD Citation
Ushiki, T. et al. (2019). Rhnull phenotype caused by a novel RHAG mutation, c.945+1G>A, in the Japanese population. Transfusion. 59 (8), pp. 2519-2522. [Online].
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Ushiki, T. et al. (2019). Rhnull phenotype caused by a novel RHAG mutation, c.945+1G>A, in the Japanese population. Transfusion. 59 (8), pp. 2519-2522. [Online].