Red Blood Cell Membrane Defects
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-030-49980-8_8
Reference7 articles.
1. Bogardus HH, Maksimova YD, Forget BG, Gallagher PG. A de novo band 3 mutation in hereditary spherocytosis. Pediatr Blood Cancer. 2012;58(6):1004.
2. Andolfo I, Russo R, Gambale A, Iolascon A. New insights on hereditary erythrocyte membrane defects. Haematologica. 2016;101(11):1284–94.
3. Bolton-Maggs P, Langer J, Iolascon A, Tittensor P, King MJ. Guidelines for the diagnosis and management of hereditary spherocytosis – 2011 update. Br J Haematol. 2011;156:37–49.
4. Christensen RD, Yaish HM, Gallagher PG. A pediatrician’s practical guide to diagnosing and treating hereditary spherocytosis in neonates. Pediatrics. 2015;135(6):1107–14.
5. An X, Mohandas N. Disorders of red cell membrane. Br J Haematol. 2008;141:367.
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