Diagnosing PNH with FLAER and Multiparameter Flow Cytometry: Our Experiences in Apollo Hospitals Dhaka
Mizanur Rahman, Rummana Rahim, Abu Hasan Paroxysmal nocturnal haemoglobinuria (PNH) is a rare stem cell disorder caused by acquired mutation in the X-linked phosphatidylinositol glycan complementation class A gene. The acquired mutation generates a defect in the expression of glycol-phosphatidyl … Continue reading →