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Article

Molecular basis of Bombay phenotype in Mashhad, Iran: identification of a novel FUT1 deletion.

Vox sanguinis - 1 Jul 2016

Zanjani D S, Afzal Aghaee M, Badiei Z, Mehrasa R, Roodsarabi A, Khayyami M E, Shahabi M

Abstract excerpt

BACKGROUND AND OBJECTIVES: Bombay phenotype is characterized by the lack of H substance both on red blood cell (RBC) surface and in body secretions. Mutations of fucosyltransferase 1 (FUT1) and fucosyltransferase 2 (FUT2) genes are resulted in this rare phenotype. MATERIALS AND METHODS: Five unrelated patients were tested by hemagglutination and adsorption/elution techniques for the presence of ABH antigens. The...

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Source

Identifiers

PMID: 26926997
DOI: 10.1111/vox.12393

Genes

FUT1
FUT2
ABO

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.

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Molecular basis of Bombay phenotype in Mashhad, Iran: identification of a novel FUT1 deletion.PMID 26926997Read ↗

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