首页> Frontiers in genetics> Case Report: identification of a novel 9.159-kb deletion in a Chinese α-thalassemia family using single molecule real-time technology sequencing.

Case Report: identification of a novel 9.159-kb deletion in a Chinese α-thalassemia family using single molecule real-time technology sequencing.

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第一作者： Shulin,Wu

第一单位： Neonatal Disease Screening Center, Huaihua City Maternal and Child Healthcare Hospital, Huaihua, Hunan, China.

作者： Shulin,Wu ^[1] ; Zonghui,Feng ^[1] ; Fuxiang,Jiang ^[1] ; Min,Zhao ^[1] ; Peng,Jiang ^[1] ; Gang,Xiao ^[1] ; Xian,Zhang ^[1]

作者单位： Neonatal Disease Screening Center, Huaihua City Maternal and Child Healthcare Hospital, Huaihua, Hunan, China. ^[1]

关键词 HBA2 gene SMRT deletion rare variant α-thalassemia

DOI 10.3389/fgene.2025.1669814

PMID 41262547

发布时间 2025-11-22

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Frontiers in genetics

2025年16卷

1669814页

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Case Report: identification of a novel 9.159-kb deletion in a Chinese α-thalassemia family using single molecule real-time technology sequencing.

Frontiers in genetics

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Case Report: identification of a novel 9.159-kb deletion in a Chinese α-thalassemia family using single molecule real-time technology sequencing.

Frontiers in genetics

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Frontiers in genetics

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