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Article Dans Une Revue Transfusion Année : 2019

Functional analysis of novel RHD variants: splicing disruption is likely to be a common mechanism of variant D phenotype

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hal-02343205 , version 1 (02-11-2019)

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Loann Raud, Chandran Ka, Isabelle Gourlaouen, Isabelle Callebaut, Claude Férec, et al.. Functional analysis of novel RHD variants: splicing disruption is likely to be a common mechanism of variant D phenotype. Transfusion, 2019, 59 (4), pp.1367-1375. ⟨10.1111/trf.15210⟩. ⟨hal-02343205⟩
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