Associated Papers
New insights on hereditary erythrocyte membrane defects.
Andolfo I et al.
Haematologica, 2016
The molecular basis of hereditary red cell membrane disorders.
Delaunay J
Blood Reviews, 2007
Different impacts of alleles alphaLEPRA and alphaLELY as assessed versus a novel, virtually null allele of the SPTA1 gene in trans.
Delaunay J et al.
British Journal of Haematology, 2004
Hereditary spherocytosis: from clinical to molecular defects.
Iolascon A et al.
Haematologica, 1998
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