Ankyrin-linked hereditary spherocytosis in an African-American kindred
Author:
Publisher
Wiley
Subject
Hematology
Reference63 articles.
1. Hereditary spherocytosis-Defects in proteins that connect the membrane skeleton to the lipid bilayer;Eber;Semin Hematol,2004
2. Organizing the fluid membrane bilayer: Diseases linked to spectrin and ankyrin;Bennett;Trends Mol Med,2008
3. Ankyrin deficiency is the most common defect in dominant and non dominant hereditary spherocytosis;Lanciotti;Haematologica,1997
4. Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis;Lee;J Korean Med Sci,2000
5. Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis;Miraglia del Giudice;Br J Haematol,1994
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1. Forward Genetics in Apicomplexa Biology: The Host Side of the Story;Frontiers in Cellular and Infection Microbiology;2022-05-12
2. A previously unrecognized Ankyrin‐1 mutation associated with Hereditary Spherocytosis in an Italian family;European Journal of Haematology;2019-08-27
3. Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis;Science China Life Sciences;2018-03-19
4. Spectrum of Ankyrin Mutations in Hereditary Spherocytosis: A Case Report and Review of the Literature;Acta Haematologica;2018
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