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Article

Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease.

Experimental hematology - 1 Nov 2001

Dekker J, de Boer M, Roos D

Abstract excerpt

OBJECTIVE: We devised a method to recognize carriers and patients with p47(phox)-deficient chronic granulomatous disease (A47 CGD), the most common autosomal form of the disease. CGD is characterized by the inability of phagocytic leukocytes to kill microorganisms, due to a defective NADPH oxidas...

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Share to Genes, Recessive
Share to Genetic Carrier Screening
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Granulomatous Disease, Chronic

Share to NADPH Oxidases

Share to Phosphoproteins

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Source

Identifiers

PMID: 11698128
DOI: 10.1016/s0301-472x(01)00731-7

Genes

NCF1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-11698128-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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