MPO383SLOT - Portal Universitas Indonesia

mpo 383Myeloperoxidase Deficiency. In 6 of 7 patients with complete MPO deficiency (), Nauseef et al. (1994) identified an arg569-to-trp mutation (R569W; 606989.0001) inMyeloperoxidase Deficiency. In 6 of 7 patients with complete MPO deficiency (), Nauseef et al. (1994) identified an arg569-to-trp mutation (R569W; 606989.0001) in