Model Pelaporan On (MPO)

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) inThe Memphis MPO assesses the development patterns in our region, then uses that information to help our cities and towns make smarter decisions about how to prioritize infrastructure