Abstract
This reference was identified in a congress abstract or in an online resource.
Weak RhD phenotype caused by compound heterozygosity for DAU-2 and a new RHD*c393-394 dupGG-mutation. Karnot A., Woestmann S.J., Flesch B.K.. Transfus Med Hemother, 2016.
Remark: vol. 43 (S1), pp. 42-43, abstract P02-19
Annotations by Allele
- RHD*209A,998A,1136T (DAU2): RH1 (heterozygous with RHef00685)
- RHD*209A,998A,1136T (DAU2): Serology (heterozygous with RHef00685)
- RHD*209A,998A,1136T (DAU2): Prevalence
- RHD*396_397insGG: Serology (heterozygous with RHef00685)
- RHD*396_397insGG: Prevalence