PNH phenotypes and their genesis
Author:
Affiliation:
1. Department of Haematology and Blood Tranfusion Muhimbili University of Health and Allied Sciences Dar‐es‐Salaam Tanzania
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.16473
Reference31 articles.
1. Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals
2. Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria
3. High incidence of thrombosis in African-American and Latin-American patients with Paroxysmal Nocturnal Haemoglobinuria
4. CD59-deficient blood cells and PIG-A gene abnormalities in Japanese patients with aplastic anaemia
5. Cooperativity of imprinted genes inactivated by acquired chromosome 20q deletions
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