Defective spectrin dimer–dimer association in a family with transfusion dependent homozygous hereditary elliptocytosis
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1983.tb02085.x/fullpdf
Reference25 articles.
1. Deficient Red-Cell Spectrin in Severe, Recessively Inherited Spherocytosis
2. Analysis of the red cell membrane in a family with hereditary elliptocytosis — total or partial of protein 4.1
3. Red cell membrane protein anomalies in congenital dyserythropoietic anaemia, type II (HEMPAS)
4. Tryptic digestion of spectrin in variants of hereditary elliptocytosis.
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