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Article

A Chinese individual with DEL phenotype caused by a novel RHD allele.

Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis - 1 Oct 2024

Wu Fan, Luo Ya-Dan, Liang Shuang, Sun Li-Yan, Liu Tong, Liang Yan-Lian, Su Yu-Qing

Abstract excerpt

BACKGROUND: RhD variants are categorized into partial D, weak D, and DEL. The detection of DEL can only be achieved through the adsorption and elution method or molecular techniques. Here, we report a case of DEL phenotypes associated with a novel allele in a Chinese individual. STUDY DESIGN AND METHODS: We used serological methods such as saline, indirect anti-human globulin, and adsorption-elution. The RHD...

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PMID: 39089169
DOI: 10.1016/j.transci.2024.103973

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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