Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia

Abstract Abnormal hemoglobin anti-Lepore Hong Kong is a rare βδ fusion variants resulting from non-homologous crossover during meiosis. Anti-Lepore Hong Kong is known to consistently exhibit significantly increased level of HbA2. In this study, we used multiplex ligation-dependent probe amplificatio...

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Hlavní autoři:	Xiuqin Bao, Jicheng Wang, Danqing Qin, Cuize Yao, Jie Liang, Kailing Liang, Li Du
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Nature Portfolio 2024-03-01
Edice:	Scientific Reports
Témata:	Anti-Lepore Hong Kong Increased HbA2 Anti-Lepore Hong Kong compounded with β0-thalassemia and α-thalassemia Single molecular real time sequencing
On-line přístup:	https://doi.org/10.1038/s41598-024-56921-6
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