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Article

Molecular basis of DEL phenotype in the Indian population: Insights from next-generation sequencing analysis of two cases.

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

Rophina Mercy, Sinha Ayesha, Biswas Durba, Basu Debapriya, Datta Suvro Sankha, Scaria Vinod

Abstract excerpt

The DEL phenotype represents an intriguing and challenging aspect of blood group serology. This condition is characterized by an extremely weak expression of the D antigen on red blood cells, to the extent that it often eludes detection through routine serological methods. Identifying the DEL phenotype necessitates more specialized techniques, such as adsorption and elution tests, to reveal the presence of the D...

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PMID: 38272782
DOI: 10.1016/j.transci.2024.103872

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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