MYELOPEROXIDASE DEFICIENCY: SINGLE CENTER EXPERIENCE
Objective: Myeloperoxidase (MPO) is a hemoprotein expressed in azurophilic granules of neutrophils and lysosomes of monocytes. It is caused by mutations in the MPO gene on chromosome 17 and is estimated to affect 1:2000-4000 people. It is the most common inherited defect of phagocytes. Microbial kil...
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| Main Authors: | , |
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| Format: | article |
| Language: | EN |
| Published: |
Elsevier
2021
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| Subjects: | |
| Online Access: | https://doaj.org/article/7789f8a1c3e1409b9699deeae3d05c79 |
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