Serological weak D phenotype caused by a novel RHD variant allele with a nucleotide change (c. 283G >T)
Abstract
The authors have disclosed no conflicts of interest. Research data are not shared. TABLE S1. The primer sequences and their respective concentrations for TGS. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Fields of Study & Subjects
Blood groups and transfusion
Blood transfusion and management
Hemoglobinopathies and Related Disorders
Publication details
- Journal / source
- Transfusion
- Volume
- 66
- Issue
- 2
- Pages
- 415–417
- Publication date
- 20 January 2026
- Language
- EN