Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease-Reference-Cited by-同舟云学术

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Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease

Published:2015-09-15 Issue:1 Volume:40 Page:64-65
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Akinbami Anthony O.,Campbell Andrew D.,Han Zeqiu J.,Luo Hong-Yuan,Chui David H.K.,Steinberg Martin H.

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1080725

Reference9 articles.

1. Pathogenesis and Treatment of Sickle Cell Disease

2. Fetal hemoglobin in sickle cell anemia

3. Molecular and cellular pathogenesis of hemoglobin SC disease.

4. Ligand state of intraerythrocytic circulating HbC crystals in homozygote CC patients

5. Clinical, hematological, and biochemical features of Hb SC disease

Cited by 5 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. HbSC disease: A time for progress;American Journal of Hematology;2022-09-08

2. Fetal Hemoglobin in Sickle Hemoglobinopathies: High HbF Genotypes and Phenotypes;Journal of Clinical Medicine;2020-11-23

3. Fetal Hemoglobin Modulators May Be Associated With Symptomology of Football Players with Sickle Cell Trait;Southern Medical Journal;2019-05

4. Krüppel-Like Factor 1Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia;Hemoglobin;2019-01-02

5. Human hemoglobin G-Makassar variant masquerading as sickle cell anemia;Hematology Reports;2018-09-24

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