Serological weak D phenotype caused by a novel RHD variant allele with a nucleotide change (c. 283G >T)
Year: 2026
Type: article
Source: Transfusion
DOI: 10.1111/trf.70041
Authors: Jue Hou, Yuwei Zhao, Meng Li, Xue Chen
Language: English
Topic: Blood groups and transfusion
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W7124938682