Point mutation in the band 4.2 gene associated with autosomal recessively inherited erythrocyte band 4.2 deficiency
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1993.tb00164.x/fullpdf
Reference33 articles.
1. Red cell membrane skeletal defects in hereditary and acquired hemolytic anemias;Palek;Semin Hematol,1983
2. Spectrin Tunis (SpαI/78), an elliptocytogcnic variant, is due to the CGG& RR; TGG codon change (Arg& RR; Trp) at position 35 of the α I domain;Morle;Blood,1989
3. Structural and functional heterogeneity of a spectrin mutations involving the spectrin heterodimer self-association site: Relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis;Coetzer;Blood,1990
4. An insertional frameshift mutation of the β-spectrin gene associated with elliptocytosis in spectrin Nice (β220/216);Tse;Blood,1991
5. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8;Lux;Nature,1990
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1. Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China;Annals of Hematology;2018-07-01
2. Hereditary Disorders of the Red Cell Membrane;Postgraduate Haematology;2010-11-16
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. Induction of Erythrocyte Protein 4.2 Gene Expression during Differentiation of Murine Erythroleukemia Cells;Genomics;1999-07
5. Electron microscopic evidence of impaired intramembrane particles and instability of the cytoskeletal network in band 4.2 deficiency in human red cells;Cell Motility and the Cytoskeleton;1996
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