XmnI Polymorphism in Sickle Cell Disease in North Morocco
Author:
Affiliation:
1. Biomedical Genomics and Oncogenetics Research Laboratory, Faculty of Sciences and Techniques of Tangier, University Abdelmalek Essaadi, Tangier, Morocco
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1772284
Reference38 articles.
1. Discovering the genetics underlying foetal haemoglobin production in adults
2. The inherited diseases of hemoglobin are an emerging global health burden
3. Un tératome nasopharyngé extensif
4. Sickle cell disease
5. The Natural History of Sickle Cell Disease
Cited by 2 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. Genetic Variation and Sickle Cell Disease Severity;JAMA Network Open;2023-10-18
2. The HBG2 rs7482144 (C > T) Polymorphism is Linked to HbF Levels but not to the Severity of Sickle Cell Anemia;Journal of Pediatric Genetics;2021-08-31
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