Altered membrane phospholipid organization and erythrophagocytosis in Eβ-thalassemia
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Biochemistry,Biophysics
Reference36 articles.
1. Identification of five rare mutations including a novel frameshift mutation causing β0-thalassemia in Thai patients with β0-thalassemia/hemoglobin E disease
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3. Differing erythrocyte membrane skeletal protein defects in alpha and beta thalassemia.
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5. Loss of phospholipid membrane asymmetry and sialylated glycoconjugates from erythrocyte surface in haemoglobin E β-thalassaemia;British Journal of Haematology;2008-04
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