Hereditary eosinophil peroxidase deficiency: immunochemical and spectroscopic studies and evidence for a compound heterozygosity of the defect.

Hereditary eosinophil peroxidase (EPO; EC 1.11.1.7) deficiency is a rare abnormality of eosinophil granulocytes characterized by decreased or absent peroxidase activity and decreased volume of the granule matrix. The molecular basis of the defect is not known. We report here its molecular characteri...

Whakaahuatanga katoa

Ngā taipitopito rārangi puna kōrero

I whakaputaina i:	Proc Natl Acad Sci U S A
Ngā kaituhi matua:	Romano, M, Patriarca, P, Melo, C, Baralle, F E, Dri, P
Hōputu:	Artigo
Reo:	Inglês
I whakaputaina:	National Academy of Sciences 1994
Ngā marau:	Research Article
Urunga tuihono:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC45465/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7809065/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.91.26.12496
Ngā Tūtohu:	Tāpirihia he Tūtohu Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!