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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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Dettagli Bibliografici
Pubblicato in:Mol Genet Genomic Med
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2019
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Accesso online: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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