Compounded with hemoglobin Port Phillip and ‐α4.2 or ‐‐SEA deletions were identified in Chinese population

ConclusionHere we first time identified two patients compound with Hb Port Phillip and - α4.2 and --SEA deletions, respectively, which had never been reported. Our study widens the genotypes of hemoglobinopathy and provides reference for genetic counselling and prenatal diagnosis in this population.

Source: Molecular Genetics & Genomic Medicine - August 16, 2021 Category: Genetics & Stem Cells Authors: Li Du, Xiuqin Bao, Danqing Qin, Jicheng Wang, Cuize Yao, Jie Liang, Jianhong Chen, Aihua Yin Tags: CLINICAL REPORT Source Type: research