Coinheritance of beta-thalassemia minor and hereditary pyropoikilocytosis: case report
Author:
Publisher
Elsevier BV
Subject
Hematology,Immunology and Allergy
Reference7 articles.
1. Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis;Hanspal;Blood,1993
2. Crystal structure and functional interpretation of the erythrocyte spectrin tetramerization domain complex;Ipsaro;Blood,2010
3. Genotype–phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis;Niss;Blood Cells Mol Dis,2016
4. Frequencies of CD39, IVS1-1, IVS1-6 and IVS1-110 mutations in beta-thalassemia carriers and their influence on hematimetric indices;Gomes;J Bras Patol Med Lab,2017
5. Hereditary pyropoikilocytosis: a rare but potentially severe form of congenital hemolytic anemia;Ramos;J Pediatr Hematol Oncol,2007
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1. Unravelling the genetic and phenotypic heterogeneity of SPTA1 gene variants in Hereditary Elliptocytosis and Hereditary Pyropoikilocytosis patients using next-generation sequencing;Gene;2022-11
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