Identification of a novel <i>RHD*404T</i> allele in a Chinese individual with variant D phenotype

The authors have disclosed no conflicts of interest. The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions. Figure S1. Identification of a homozygous missense mutation in the exon 3 of the RHD gene in a Chinese woman with partial D phenotype. The mutant sequence and the corresponding wild-type sequence are shown. The codons with the missense mutation and the corresponding wild-type nucleotides are underlined. 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.