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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Detalhes bibliográficos
Publicado no:Mol Genet Genomic Med
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
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Original Articles
Acesso em linha: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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