The diagnosis and characterization of Waldenström's macroglobulinemia

Ramón Garcia Sanz, MD, PhD, Hospital Universitario de Salamanca, Salamanca, Spain, discusses the diagnosis and characterization of Waldenström's macroglobulinemia (WM), highlighting the importance of identifying patients with specific genetic mutations (MYD88, CXCR4, TP53) to allow for appropriate disease management. This interview took place at the 29th Congress of the European Hematology Association (EHA) in Madrid, Spain.
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