Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan.
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Cited by 97 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. Clinical, laboratory, and molecular characteristics of a cohort of children with hemoglobinopathy S/beta-thalassemia;Hematology, Transfusion and Cell Therapy;2023-12
2. Beta Globin Gene Cluster Haplotypes in Beta Thalassemia in the Kurdistan Region of Iraq;Hemoglobin;2023-05-04
3. Mutation Spectrum of β-Thalassemia in Some Ethnic Groups of North Maharashtra, India;Hemoglobin;2023-05-04
4. Mitochondrial DNA haplogroup study: residents of Sulaymaniyah city in the Iraqi Kurdistan Region may be genetically closer to European lineage;Egyptian Journal of Forensic Sciences;2021-11-04
5. Mutations in cis that affect mRNA synthesis, processing and translation;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2021-09
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