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Compounded with hemoglobin Port Phillip and -α4.2 or --SEA deletions were identified in Chinese population
Molecular Genetics & Genomic Medicine ( IF 1.5 ) Pub Date : 2021-08-16 , DOI: 10.1002/mgg3.1699 Li Du 1, 2, 3, 4 , Xiuqin Bao 1, 2, 3, 4 , Danqing Qin 1, 2, 3, 4 , Jicheng Wang 1, 2, 3, 4 , Cuize Yao 1, 2, 3, 4 , Jie Liang 1, 2, 3, 4 , Jianhong Chen 5 , Aihua Yin 1, 2, 3, 4
Molecular Genetics & Genomic Medicine ( IF 1.5 ) Pub Date : 2021-08-16 , DOI: 10.1002/mgg3.1699 Li Du 1, 2, 3, 4 , Xiuqin Bao 1, 2, 3, 4 , Danqing Qin 1, 2, 3, 4 , Jicheng Wang 1, 2, 3, 4 , Cuize Yao 1, 2, 3, 4 , Jie Liang 1, 2, 3, 4 , Jianhong Chen 5 , Aihua Yin 1, 2, 3, 4
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Although over 1000 hemoglobin (Hb) variants were identified so far, Hb Port Phillip compound with α-thalassemia deletion had no reported before.
更新日期：2021-09-23
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