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Article

A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran.

Iranian journal of allergy, asthma, and immunology - 1 Oct 2016

Tajik Shaghayegh, Badalzadeh Mohsen, Fazlollahi Mohammad Reza, Houshmand Massoud, Zandieh Fariborz, Khandan Shamim, Pourpak Zahra

Abstract excerpt

Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder due to a genetic defect in one of the components of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex. This complex is composed of membrane-bound gp91-phox and p22-phox subunits, and cytosolic subunits consisting of p47-phox, p67-phox, and p40-phox. A mutation in CYBB gene encoding gp91-phox located on chromosome...

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Source

Identifiers

PMID: 27917630

Genes

CYBB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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