A de novo band 3 mutation in hereditary spherocytosis
Author:
Publisher
Wiley
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Reference9 articles.
1. Hereditary spherocytosis;Perrotta;Lancet,2008
2. Mutations of conserved arginines in the membrane domain of erythroid Band 3 lead to a decrease in membrane-associated Band 3 and to the phenotype of hereditary spherocytosis;Jarolim;Blood,1995
3. Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population;Yawata;Int J Hematol,2000
4. Molecular and haematological studies of four families with hereditary spherocytosis resulting from Band 3 deficiency;Maciag;Acta Haematol,2006
5. Arginine 490 is a hot spot for mutation in the band 3 gene in hereditary spherocytosis;Lima;Eur J Haematol,1999
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3. COVID‐19 and hereditary spherocytosis: A recipe for hemolysis;Pediatric Blood & Cancer;2020-07-25
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