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

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: A total...

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Vydáno v:Mol Genet Genomic Med
Hlavní autoři: Zhang, Jie, Yang, Yang, Li, Peng, Yan, Yuanlong, Lv, Tao, Zhao, Tingting, Zeng, Xiaohong, Li, Dongmei, Zhou, Xiaoyan, Chen, Hong, Su, Jie, Yang, Tonghua, He, Jing, Zhu, Baosheng
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2019
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6565566/
https://ncbi.nlm.nih.gov/pubmed/31044540
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.706
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