Hereditary spherocytosis is a condition that affects red blood cells.
genetic conditions
References
Eber S, Lux SE. Hereditary spherocytosis--defects in proteins that connect themembrane skeleton to the lipid bilayer. Semin Hematol. 2004 Apr;41(2):118-41.Review.
Iolascon A, Avvisati RA, Piscopo C. Hereditary spherocytosis. Transfus ClinBiol. 2010 Sep;17(3):138-42. doi: 10.1016/j.tracli.2010.05.006.
Iolascon A, Avvisati RA. Genotype/phenotype correlation in hereditaryspherocytosis. Haematologica. 2008 Sep;93(9):1283-8. doi: 10.3324/haematol.13344.
Mariani M, Barcellini W, Vercellati C, Marcello AP, Fermo E, Pedotti P,Boschetti C, Zanella A. Clinical and hematologic features of 300 patientsaffected by hereditary spherocytosis grouped according to the type of themembrane protein defect. Haematologica. 2008 Sep;93(9):1310-7. doi:10.3324/haematol.12546.
Narla J, Mohandas N. Red cell membrane disorders. Int J Lab Hematol. 2017May;39 Suppl 1:47-52. doi: 10.1111/ijlh.12657. Review.
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