Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China

Abstract Background Deletional hereditary persistence of fetal hemoglobin (HPFH)/δβ‐thalassemia and δ‐thalassemia are rare inherited disorders which may complicate the diagnosis of β‐thalassemia. The aim of this study was to reveal the frequency of these two disorders in Southwestern China. Methods...

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Hauptverfasser:	Jie Zhang, Yang Yang, Peng Li, Yuanlong Yan, Tao Lv, Tingting Zhao, Xiaohong Zeng, Dongmei Li, Xiaoyan Zhou, Hong Chen, Jie Su, Tonghua Yang, Jing He, Baosheng Zhu
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Wiley 2019-06-01
Schriftenreihe:	Molecular Genetics & Genomic Medicine
Schlagworte:	bioinformatics analysis capillary electrophoresis hereditary persistence of fetal hemoglobin δ‐thalassemia
Online-Zugang:	https://doi.org/10.1002/mgg3.706
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