Functional investigation of the <scp> <i>RHD</i> </scp> gene promoter: Molecular changes are rarely responsible for variant D phenotype in Thai donors
Regulation of RH gene expression is likely to involve other levels of complexity that remain to be identified. Future investigations are necessary to characterize those critical genomic regions that potentially carry rare variants responsible for weakening or abolishment of D antigen expression.
Authors
- Yann Fichou (ORCID: https://orcid.org/0000-0002-5104-9125)
- Pornlada Nuchnoi (ORCID: https://orcid.org/0000-0002-1123-1037)
Institutions
- Inserm (FR)
- Université de Bretagne Occidentale (FR)
- École nationale d'ingénieurs de Brest (FR)
- Mahidol University (TH)
- Génétique, Génomique Fonctionnelle et Biotechnologies (FR)
Publication Details
- Journal
- Transfusion
- Published
- 2026-03-07
- DOI
- https://doi.org/10.1111/trf.70155
- Primary Topic
- Blood groups and transfusion
- Type
- article
- Field-Weighted Citation Impact
- 0.00