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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565566/
https://www.ncbi.nlm.nih.gov/pubmed/31044540
http://dx.doi.org/10.1002/mgg3.706

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565566/
https://www.ncbi.nlm.nih.gov/pubmed/31044540
http://dx.doi.org/10.1002/mgg3.706

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