Eosinophil peroxidase deficiency is a condition caused by mutations of the EPX gene. The pathogenic relevance is still under discussion. Some researchers assume a connection with food intolerance.
1. |
Romano M et al. (1994) Hereditary eosinophil peroxidase deficiency: immunochemical and spectroscopic studies and evidence for a compound heterozygosity of the defect. |
2. |
Nakagawa T et al. (2001) Eosinophilic peroxidase deficiency: Identification of a point mutation (D648N) and prediction of structural changes. |
3. |
Zabucchi G et al. (1992) Eosinophil peroxidase deficiency: morphological and immunocytochemical studies of the eosinophil-specific granules. |
4. |
Lepelley P et al. (1987) Total peroxidase deficiency in eosinophils: a report on twin sisters, one with a refractory anaemia. |
5. |
Valdés MD et al. (1987) Deficiency of eosinophil peroxidase detected by automated cytochemistry. |
6. |
Lejeune F et al. (1988) [Peroxidase deficiency in eosinophils: an optical and electron microscopy cytologic study apropos of a case]. |
7. |
Hoffmann JJ et al. (1987) Partial deficiency of eosinophil peroxidase. |
8. |
Presentey B et al. (1969) Hereditary deficiency of peroxidase and phospholipids in eosinophilic granulocytes. |
9. |
None (1970) Partial and severe peroxidase and phospholipid deficiency in eosinophils. Cytochemical and genetic considerations. |
10. |
None (1969) Morphologic observations and genetic follow-up of a familial anomaly of eosinophils. |
11. |
Presentey B et al. (1982) Peroxidase and phospholipid deficiency in human eosinophilic granulocytes--a marker in population genetics. |
12. |
None (1984) Ultrastructure of human eosinophils genetically lacking peroxidase. |
13. |
OMIM.ORG article Omim 261500 |