Severe hemolysis and red cell fragmentation caused by the combination of a spectrin mutation with a thrombotic microangiopathy
Author:
Publisher
Wiley
Subject
Hematology
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3. Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin αI variants;British Journal of Haematology;2008-03-12
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5. Hereditary elliptocytosis: spectrin and protein 4.1R;Seminars in Hematology;2004-04
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