Advances in understanding the pathogenesis of red cell membrane disorders
Author:
Affiliation:
1. Department of Molecular Medicine and Medical Biotechnologies Federico II” University of Naples NaplesItaly
2. CEINGE – Biotecnologie Avanzate Naples Italy
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.16126
Reference110 articles.
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4. Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low‐expression allele occurring in trans (allele Genas);Alloisio N.;Blood,1996
5. Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis
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