Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis-Reference-Cited by-同舟云学术

Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis

Published:2016-10 Issue: Volume:61 Page:4-9
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Niss Omar,Chonat Satheesh,Dagaonkar Neha,Almansoori Marya O.,Kerr Karol,Rogers Zora R.,McGann Patrick T.,Quarmyne Maa-Ohui,Risinger Mary,Zhang Kejian,Kalfa Theodosia A.

Funder

National Center for Advancing Translational Sciences of the National Institutes of Health

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference21 articles.

1. Hereditary elliptocytosis: spectrin and protein 4.1R;Gallagher;Semin. Hematol.,2004

2. Interactions of the alpha-spectrin N-terminal region with beta-spectrin. Implications for the spectrin tetramerization reaction;Cherry;J. Biol. Chem.,1999

3. Crystal structure and functional interpretation of the erythrocyte spectrin tetramerization domain complex;Ipsaro;Blood,2010

4. Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders;Da Costa;Blood Rev.,2013

5. Disorders of red cell membrane;An;Br. J. Haematol.,2008

Cited by 58 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Frameshift Mutation in the EPB41 Gene with Hereditary Elliptocytosis;Indian Journal of Hematology and Blood Transfusion;2024-09-14

2. Hereditary spherocytosis due to a novel variant, p.Q1034X, in the beta subunit of the spectrin gene: A case report;Pediatric Hematology Oncology Journal;2024-09

3. Cytoskeletal Protein 4.1R in Health and Diseases;Biomolecules;2024-02-11

4. Hämatologie in der pädiatrischen Praxis;Kinder- und Jugendmedizin;2024-02

5. Hereditary Pyropoikilocytosis;Decision Making Through Problem Based Learning in Hematology;2024