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Article

A Bombay individual lacking H and Le antigens but expressing normal levels of alpha-2- and alpha-4-fucosyltransferases.

Transfusion - 1 Sept 1995

Shechter Y, Etzioni A, Levene C, Greenwell P

Abstract excerpt

BACKGROUND: The rare Bombay phenotype is usually due to a primary genetic defect in an alpha-2- or alpha-4-fucosyltransferase. The present study was done to investigate a patient with normal transferases, who exhibits the Bombay phenotype. CASE REPORT: Red cells of the patient, his parents, and siblings were phenotyped for A, B, and H antigens. The presence of B, H, and Le transferases in serum and saliva was...

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Source

Identifiers

PMID: 7570940
DOI: 10.1046/j.1537-2995.1995.35996029164.x

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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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A Bombay individual lacking H and Le antigens but expressing normal levels of alpha-2- and alpha-4-fucosyltransferases.PMID 7570940Read ↗

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c.49T>C mutation on the α-(1,2)-fucosyltransferase gene responsible for an individual with para-Bombay phenotype.Semantic proximity Read ↗

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Incidental Discovery of a Patient with the Bombay Phenotype.Semantic proximity Read ↗

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