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Article

Genetic studies on myeloperoxidase deficiency in Italy.

Japanese journal of infectious diseases - 1 Oct 2004

Marchetti Caterina, Patriarca Pierluigi, Solero G Pietro, Baralle Francisco E, Romano Maurizio

Abstract excerpt

Hereditary myeloperoxidase (MPO) deficiency is the most common neutrophil biochemical defect characterized by the lack of peroxidase activity. In order to extend the epidemiological studies on hereditary MPO deficiency in Italy, approximately 40,000 individuals were analyzed and 7 partial and 8 total MPO deficient subjects were identified. The genetic characterization of the subjects showed the presence of 3...

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PMID: 15507752

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MPO

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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