Characterization of genetic variation in promotors of HBG1 and HBG2 gene
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https://www.ncbi.nlm.nih.gov/sra/SRP444749
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资源简介：
Polymorphism occurring in the HBG2 gene on chromosome 11 is an inherent modifier in beta-thalassemia which is strongly associated with increased HbF expression in beta-thal diseases, sickle cell disease, and healthy individuals
创建时间：
2023-09-01
