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Study on Hb H disease caused by the α2-globin gene initiation codon ATG > GTG mutation combined with Southeast Asian deletional α-thalassemia

Objective To explore the hemoglobin H (Hb H) diseases diseases caused by a rare α2-globin gene mutation combined with the Southeast Asian deletion of α -thalassemia gene mutation. Methods For the suspected cases of Hb H disease screened in the First Affiliated Hospital of Guangxi Medical University...

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Principais autores: Xiaobi LIU, Xuan XIAO, Hengying ZHU, Ping CHEN
Format: Artigo
Sprog:Chinês
Udgivet: Editorial Office of Journal of Guangxi Medical University 2025-06-01
Serier:Guangxi Yike Daxue xuebao
Fag:
α-thalassemia
hb h disease
α2-globin gene
initiation codon
atg > gtg mutation
Online adgang:https://journal.gxmu.edu.cn/article/doi/10.16190/j.cnki.45-1211/r.2025.03.012
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