Erythrocyte membrane defects and asymmetry in paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome
Author:
Affiliation:
1. Structural Genomics SectionSaha Institute of Nuclear Physics, Kolkata, India
2. Department of PathologyRamakrishna Mission Seva Prathisthan, Kolkata, India
3. Department of HaematologyNilratan Sarkar Medical College, Kolkata, India
Publisher
Informa UK Limited
Subject
Hematology,Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1179/102453309X12583347114095
Reference16 articles.
1. Deficiency of an erythrocyte membrane protein with complement regulatory activity in paroxysmal nocturnal hemoglobinuria.
2. Somatic Mutations in Paroxysmal Nocturnal Hemoglobinuria: A Blessing in Disguise?
3. The WHO classification of MDS does make a difference
4. Diagnosis and classification of myelodysplastic syndrome: International Working Group on Morphology of myelodysplastic syndrome (IWGM-MDS) consensus proposals for the definition and enumeration of myeloblasts and ring sideroblasts
5. Paroxysmal nocturnal haemoglobinuria clones in patients with myelodysplastic syndromes
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