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    Development and validation of mPCR-CEFA for detecting multiple deletion and non-deletion thalassemia genotypes

    Development and validation of mPCR-CEFA for detecting multiple deletion and non-deletion thalassemia genotypes mā Jingping Xu, Jingping Xu, Baoyan Ren, Qixun Fang, Kangfeng Lin, Kangfeng Lin, Xingan Xing, Xingan Xing, Jingting Lin

    I whakaputaina 2025-07-01

    BackgroundThalassemia is a common hereditary blood disorder caused by genetic variants in globin genes, leading to abnormal hemoglobin production. Rapid and accurate genotyping is essential for molecular screening and prenatal genetic diagnosis to prevent the birth of individuals with severe forms o...

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