Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1991.tb04487.x/fullpdf
Reference21 articles.
1. Partial deficiency of erythrocyte spectrin in hereditary spherocytosis
2. Deficient Red-Cell Spectrin in Severe, Recessively Inherited Spherocytosis
3. Human erythrocyte ankyrin. Purification and properties.
4. Association of red cell spherocytosis with deletion of the short arm of chromosome 8
5. Partial Ankyrin and Spectrin Deficiency in Severe, Atypical Hereditary Spherocytosis
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1. Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis;Science China Life Sciences;2018-03-19
2. Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblasts;Haematologica;2016-05-31
3. A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia;British Journal of Haematology;2008-03-12
4. An 11-amino acid beta-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytes;Proceedings of the National Academy of Sciences;2007-08-22
5. Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: Effects of different membrane protein defects;American Journal of Hematology;1997-07
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