Coexistence of primary myelofibrosis and paroxysmal nocturnal hemoglobinuria clone with jak2 v617f, u2af1 and setbp1 mutations: A case report and brief review of literature

Medicine and Dentistry

• Myeloid metaplasia 100%
• Paroxysmal Nocturnal Hemoglobinuria 100%
• Disease 60%
• Gene Mutation 40%
• Neoplasm 20%
• Genetic Association 20%
• Rare Disease 20%
• Next Generation Sequencing 20%
• Janus Kinase 20%

Biochemistry, Genetics and Molecular Biology

• Gene Mutation 100%
• Next Generation Sequencing 50%
• Clonal Evolution 50%
• Myeloid 50%
• Genetic Association 50%
• Janus Kinase 50%