A Chinese individual with DEL phenotype caused by a novel RHD allele.
Fan WuYa-Dan LuoShuang LiangLi-Yan SunTong LiuYan-Lian LiangYu-Qing SuPublished in: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis (2024)
Our study demonstrates a case of a Chinese individual with DEL phenotype caused by a novel allele RHD c .1127 T > G. It expands the database of the DEL variant.
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