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Article

Mutations that diminish expression of Kell surface protein and lead to the Kmod RBC phenotype.

Transfusion - 1 Aug 2003

Lee Soohee, Russo David C W, Reid Marion E, Redman Colvin M

Abstract excerpt

BACKGROUND: Kmod is an inherited rare RBC phenotype characterized by weak but detectable expression of high-incidence Kell antigens. STUDY DESIGN AND METHODS: The 19 exons and the intron-exon regions of the KEL gene from four unrelated Kmod individuals were sequenced and compared to wild-type KEL. To study the mechanisms by which the mutations result in depression of Kell antigens, mutant and wild-type Kell...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12869119
DOI: 10.1046/j.1537-2995.2003.00472.x

Genes

KEL

Variants

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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Mutations that diminish expression of Kell surface protein and lead to the Kmod RBC phenotype.PMID 12869119Read ↗

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