![](/img/cover-not-exists.png)
Functional analysis of novel RHD variants: splicing disruption is likely to be a common mechanism of variant D phenotype
Raud, Loann, Ka, Chandran, Gourlaouen, Isabelle, Callebaut, Isabelle, Férec, Claude, Le Gac, Gérald, Fichou, YannLanguage:
english
Journal:
Transfusion
DOI:
10.1111/trf.15210
Date:
February, 2019
File:
PDF, 660 KB
english, 2019