Abstract
This reference was identified in a congress abstract or in an online resource.
A novel RHD splice donor site mutation leading to a RhD-negative phenotype. C von Arx, J Stettler, J Graber, S Lejon Crottet, H Hustinx, F Still, C Niederhauser and C Henny. Vox Sanguinis, 2019.
Remark: vol. 114 (S1), pp. 184.0, abstract P-372
Annotations by Allele
- RHD*148+2delT (IVS1+2delT): Serology
- RHD*148+2delT (IVS1+2delT): Prevalence
- RHD*148+2delT (IVS1+2delT): RH1 (adsorption-elution was performed)