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Article

Molecular genetics of peroxidase deficiency.

Journal of molecular medicine (Berlin, Germany) - 1 Sept 1998

Petrides P E

Abstract excerpt

Myeloperoxidase (MPO) belongs to a family of related proteins which also includes eosinophil, thyroid, and lactoperoxidase. The MPO gene is a 14-kb gene located on the long arm of chromosome 17. Thus far four mutations (R569W, Y173C, M251T and a 14-base deletion in exon 9) have been identified in patients with MPO deficiency. As in other genetically determined diseases, many more mutations will eventually be...

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Source

Identifiers

PMID: 9766847
DOI: 10.1007/s001090050269

Genes

MPO
EPO

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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