Associated Papers
Functional analysis of novel RHD variants: splicing disruption is likely to be a common mechanism of variant D phenotype.
Raud L et al.
Transfusion, 2019
Definitive hematopoiesis requires Runx1 C-terminal-mediated subnuclear targeting and transactivation.
Dowdy CR et al.
Human Molecular Genetics, 2010
Select a paper to view details