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An insertion/deletion polymorphism in the KLF1 gene resulting in an In(Lu) phenotype.

Transfusion - 1 Oct 2021

Floch Aline, Vege Sunitha, Burgos Anna, Kuchma Sharon, Bell Mollie, Lomas-Francis Christine, Westhoff Connie M

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 34487547
DOI: 10.1111/trf.16648

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An insertion/deletion polymorphism in the KLF1 gene resulting in an In(Lu) phenotype.PMID 34487547Read ↗

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Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype.Semantic proximity Read ↗

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